Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001134655.1 | 731 | Missense Mutation | CGT,TGT | R106C | NP_001128127.1 |
NM_004220.2 | 731 | Missense Mutation | CGT,TGT | R106C | NP_004211.1 |
XM_011522652.2 | 731 | Missense Mutation | CGT,TGT | R106C | XP_011520954.1 |