Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_203394.2 | 2821 | Missense Mutation | CCC,CGC | P862R | NP_976328.2 |
XM_011537966.2 | 2821 | Missense Mutation | CCC,CGC | P817R | XP_011536268.1 |
XM_011537969.2 | 2821 | Missense Mutation | CCC,CGC | P761R | XP_011536271.1 |