Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286679.1 | 1278 | Missense Mutation | CGG,TGG | R272W | NP_001273608.1 |
NM_018357.3 | 1278 | Missense Mutation | CGG,TGG | R456W | NP_060827.2 |
NM_197958.2 | 1278 | Intron | NP_932062.1 |