Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022139.3 | 667 | Missense Mutation | CGG,TGG | R223W | NP_071422.1 |
NM_145762.2 | 667 | Missense Mutation | CGG,TGG | R253W | NP_665705.1 |
XM_005260793.2 | 667 | Intron | XP_005260850.1 |