Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004961.3 | 826 | Missense Mutation | TGT,TTT | C463F | NP_004952.2 |
XM_011531140.2 | 826 | Missense Mutation | TGT,TTT | C241F | XP_011529442.1 |
XM_017029386.1 | 826 | Missense Mutation | TGT,TTT | C350F | XP_016884875.1 |
XM_017029387.1 | 826 | Missense Mutation | TGT,TTT | C318F | XP_016884876.1 |
XM_017029388.1 | 826 | Missense Mutation | TGT,TTT | C270F | XP_016884877.1 |
XM_017029389.1 | 826 | UTR 3 | XP_016884878.1 |