Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114172.1 | 1332 | Missense Mutation | CGG,TGG | R411W | NP_001107644.1 |
NM_001303427.1 | 1332 | Missense Mutation | CGG,TGG | R457W | NP_001290356.1 |
NM_001303428.1 | 1332 | Missense Mutation | CGG,TGG | R428W | NP_001290357.1 |
NM_001303429.1 | 1332 | Missense Mutation | CGG,TGG | R352W | NP_001290358.1 |
NM_003629.3 | 1332 | Missense Mutation | CGG,TGG | R411W | NP_003620.3 |
XM_017002614.1 | 1332 | Missense Mutation | CGG,TGG | R411W | XP_016858103.1 |