Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001172632.1 | 631 | Missense Mutation | CGG,TGG | R173W | NP_001166103.1 |
NM_001172633.1 | 631 | Intron | NP_001166104.1 | ||
NM_002543.3 | 631 | Silent Mutation | GAC,GAT | D219D | NP_002534.1 |