Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318202.1 | 3337 | Missense Mutation | TGC,TGG | C1003W | NP_001305131.1 |
NM_013241.2 | 3337 | Missense Mutation | TGC,TGG | C977W | NP_037373.2 |
XM_006721180.1 | 3337 | Missense Mutation | TGC,TGG | C508W | XP_006721243.1 |
XM_011523043.2 | 3337 | Missense Mutation | TGC,TGG | C993W | XP_011521345.1 |
XM_011523044.1 | 3337 | Missense Mutation | TGC,TGG | C949W | XP_011521346.1 |
XM_011523045.2 | 3337 | Missense Mutation | TGC,TGG | C910W | XP_011521347.1 |