Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303124.1 | 880 | Missense Mutation | CGT,TGT | R186C | NP_001290053.1 |
NM_001303125.1 | 880 | Missense Mutation | CGT,TGT | R186C | NP_001290054.1 |
NM_032786.2 | 880 | Missense Mutation | CGT,TGT | R186C | NP_116175.1 |