Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198863.1 | 1629 | Missense Mutation | CGC,TGC | R477C | NP_001185792.1 |
NM_003915.5 | 1629 | Missense Mutation | CGC,TGC | R483C | NP_003906.2 |
NM_152925.2 | 1629 | Missense Mutation | CGC,TGC | R478C | NP_690902.1 |
NM_152926.2 | 1629 | Missense Mutation | CGC,TGC | R478C | NP_690903.1 |
NM_152927.2 | 1629 | Missense Mutation | CGC,TGC | R478C | NP_690904.1 |
NM_152928.2 | 1629 | Missense Mutation | CGC,TGC | R478C | NP_690905.1 |