Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018376.3 | 618 | Missense Mutation | CGT,TGT | R40C | NP_060846.2 |
XM_011518839.1 | 618 | Missense Mutation | CGT,TGT | R40C | XP_011517141.1 |
XM_017014889.1 | 618 | Missense Mutation | CGT,TGT | R40C | XP_016870378.1 |