Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171905.1 | 439 | Missense Mutation | CGG,TGG | R122W | NP_001165376.1 |
NM_001171906.1 | 439 | Intron | NP_001165377.1 | ||
NM_152395.2 | 439 | Missense Mutation | CGG,TGG | R168W | NP_689608.2 |