Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144756.1 | 291 | Intron | NP_001138228.1 | ||
NM_004885.2 | 291 | Missense Mutation | CGG,TGG | R65W | NP_004876.2 |
NM_053036.2 | 291 | Intron | NP_444264.1 | ||
XM_011531554.2 | 291 | Intron | XP_011529856.1 |