Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256670.1 | 519 | Missense Mutation | CGT,TGT | R20C | NP_001243599.1 |
NM_005700.4 | 519 | Missense Mutation | CGT,TGT | R20C | NP_005691.2 |
NM_130443.3 | 519 | Missense Mutation | CGT,TGT | R20C | NP_569710.2 |