[Steve Van Doorn]

72% of the viral protein is HIV. Even know the antigen (spikes) are Plasmodium Yoelii (malaria)
found here:
https://twitter.com/JCPEREZCODEX/status/1491029873338753028

The key to your question is "RNAs that are completely paired with SARS-CoV-2 S-derived miRNAs"
Reword it a little:
"SARS-CoV-2" is the viral protein. S or subunit of the derived miRNAs or S1S2 viral protein(from the injection.)
RNAs that are completely paired with SARS-CoV-2. Which means they had to sequence the subunits to match the viral protein in order for them to bond.

To match them they used SIV(GP120) and dipped it in a solution of β-propiolactone (BPL) or formaldehyde solution to inactivate their new protein. The problem was Perez and Montagnier has made other papers showing the inactivation process didn't work. The injections are mutating.

This isn't my field either. During this research I found there are a very small number of what MD doctors call "chemist" and many of them have blinders on. They must know this is how you create autoimmunity.
https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.121.318902

When you question these chemist most of them sound like the trolls on FR that distract rather then answering the question. There are a few exceptions. Find a group on twitter (many banned including me) called #CTCCTCGGCGGGCACGTAG

[absalom01]

Ah, the graphic helps. Now I think I understand what Perez is saying here. He's found a region of the viral codon 273 base pairs long, with sequences that are identical to areas also found in various strains of HIV and SIV and form 72% of the base pairs in that region, per his note on the lower right. So, mighty suspicious, still after all this time, isn't it? And thank you for taking the time to walk me through all of this. But one more thing, if you have time. You say "Even know the antigen (spikes) are Plasmodium Yoelii (malaria)". You mean that the Spike protein is similar or identical to a protein found on or in the plasmodium parasite, right?