Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297609.1 | 3976 | Missense Mutation | ACC,ATC | T1236I | NP_001284538.1 |
NM_004672.4 | 3976 | Missense Mutation | ACC,ATC | T1244I | NP_004663.3 |
XM_017002771.1 | 3976 | Missense Mutation | ACC,ATC | T825I | XP_016858260.1 |
XM_017002772.1 | 3976 | Intron | XP_016858261.1 |