Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278599.1 | 337 | Intron | NP_001265528.1 | ||
NM_001699.5 | 337 | Missense Mutation | CAG,CGG | Q48R | NP_001690.2 |
NM_021913.4 | 337 | Missense Mutation | CAG,CGG | Q48R | NP_068713.2 |