Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282205.1 | 774 | Intron | NP_001269134.1 | ||
NM_001282206.1 | 774 | Missense Mutation | CGG,TGG | R108W | NP_001269135.1 |
NM_001282207.1 | 774 | Missense Mutation | CGG,TGG | R188W | NP_001269136.1 |
NM_001282208.1 | 774 | UTR 3 | NP_001269137.1 | ||
NM_001282209.1 | 774 | UTR 3 | NP_001269138.1 | ||
NM_005866.3 | 774 | Missense Mutation | CGG,TGG | R208W | NP_005857.1 |
NM_147157.2 | 774 | Missense Mutation | CGG,TGG | R177W | NP_671513.1 |