Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009922.2 | 757 | Missense Mutation | CGT,TGT | R245C | NP_001009922.1 |
NM_001278536.1 | 757 | Missense Mutation | CGT,TGT | R214C | NP_001265465.1 |
NM_001278537.1 | 757 | Missense Mutation | CGT,TGT | R205C | NP_001265466.1 |
NM_001278538.1 | 757 | Missense Mutation | CGT,TGT | R232C | NP_001265467.1 |
NM_001278539.1 | 757 | Missense Mutation | CGT,TGT | R127C | NP_001265468.1 |
NM_015436.3 | 757 | Missense Mutation | CGT,TGT | R254C | NP_056251.2 |
XM_011531838.2 | 757 | Missense Mutation | CGT,TGT | R127C | XP_011530140.1 |
XM_011531839.2 | 757 | Missense Mutation | CGT,TGT | R127C | XP_011530141.1 |