Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_031212.3 | 1022 | Missense Mutation | ACC,ATC | T336I | NP_112489.3 |
XM_005270208.1 | 1022 | Missense Mutation | ACC,ATC | T237I | XP_005270265.1 |
XM_005270211.4 | 1022 | Missense Mutation | ACC,ATC | T237I | XP_005270268.1 |
XM_006718005.3 | 1022 | Missense Mutation | ACC,ATC | T237I | XP_006718068.1 |
XM_006718006.3 | 1022 | Intron | XP_006718069.1 | ||
XM_011540239.2 | 1022 | Missense Mutation | ACC,ATC | T246I | XP_011538541.1 |
XM_011540240.1 | 1022 | Missense Mutation | ACC,ATC | T237I | XP_011538542.1 |
XM_011540244.2 | 1022 | Intron | XP_011538546.1 | ||
XM_017016741.1 | 1022 | Missense Mutation | ACC,ATC | T237I | XP_016872230.1 |
XM_017016742.1 | 1022 | Missense Mutation | ACC,ATC | T181I | XP_016872231.1 |