Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153453.1 | 372 | Missense Mutation | CGT,TGT | R117C | NP_703154.1 |
NM_182645.3 | 372 | Missense Mutation | CGT,TGT | R117C | NP_872586.1 |
XM_005266883.2 | 372 | Missense Mutation | CGT,TGT | R117C | XP_005266940.1 |