Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001246.3 | 919 | Missense Mutation | CGG,TGG | R289W | NP_001237.1 |
NM_203468.2 | 919 | Missense Mutation | CGG,TGG | R289W | NP_982293.1 |
XM_011519212.2 | 919 | Missense Mutation | CGG,TGG | R186W | XP_011517514.1 |