Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001287147.1 | 981 | Intron | NP_001274076.1 | ||
NM_178176.3 | 981 | Missense Mutation | GCT,GGT | A271G | NP_835470.1 |
XM_005250309.3 | 981 | Missense Mutation | GCT,GGT | A271G | XP_005250366.1 |
XM_011516126.2 | 981 | Missense Mutation | GCT,GGT | A235G | XP_011514428.1 |
XM_011516127.2 | 981 | Missense Mutation | GCT,GGT | A153G | XP_011514429.1 |