Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291978.1 | 2660 | Missense Mutation | CGG,TGG | R825W | NP_001278907.1 |
NM_001291979.1 | 2660 | Intron | NP_001278908.1 | ||
NM_003703.2 | 2660 | Missense Mutation | CGG,TGG | R825W | NP_003694.1 |