Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001103149.1 | 1536 | Intron | NP_001096619.1 | ||
NM_018215.3 | 1536 | Missense Mutation | CGG,TGG | R406W | NP_060685.2 |
XM_011527067.2 | 1536 | Missense Mutation | CGG,TGG | R406W | XP_011525369.1 |