Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014415.3 | 3959 | Missense Mutation | CGC,TGC | R782C | NP_055230.2 |
XM_011512689.2 | 3959 | Missense Mutation | CGC,TGC | R717C | XP_011510991.1 |
XM_011512690.2 | 3959 | Missense Mutation | CGC,TGC | R498C | XP_011510992.1 |