Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001244937.2 | 4218 | Missense Mutation | CGG,TGG | R1349W | NP_001231866.1 |
NM_001318913.1 | 4218 | Missense Mutation | CGG,TGG | R1292W | NP_001305842.1 |
NM_002447.3 | 4218 | Missense Mutation | CGG,TGG | R1398W | NP_002438.2 |
XM_005265170.4 | 4218 | Missense Mutation | CGG,TGG | R1399W | XP_005265227.2 |
XM_011533739.2 | 4218 | Missense Mutation | CGG,TGG | R1359W | XP_011532041.1 |
XM_011533740.2 | 4218 | Missense Mutation | CGG,TGG | R1350W | XP_011532042.1 |
XM_011533741.2 | 4218 | Missense Mutation | CGG,TGG | R1330W | XP_011532043.1 |
XM_011533742.2 | 4218 | UTR 3 | XP_011532044.1 | ||
XM_011533743.2 | 4218 | Missense Mutation | CGG,TGG | R1298W | XP_011532045.1 |
XM_011533744.2 | 4218 | Missense Mutation | CGG,TGG | R1293W | XP_011532046.1 |