Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014699.3 | 1213 | Missense Mutation | CGT,TGT | R49C | NP_055514.3 |
XM_005255710.3 | 1213 | Missense Mutation | CGT,TGT | R49C | XP_005255767.1 |
XM_005255711.3 | 1213 | Missense Mutation | CGT,TGT | R49C | XP_005255768.1 |
XM_005255712.3 | 1213 | Missense Mutation | CGT,TGT | R49C | XP_005255769.1 |
XM_011545990.2 | 1213 | Missense Mutation | CGT,TGT | R49C | XP_011544292.1 |