| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286123.1 | 1799 | Missense Mutation | ACG,ATG | T460M | NP_001273052.1 |
| NM_001286125.1 | 1799 | UTR 3 | NP_001273054.1 | ||
| NM_005835.3 | 1799 | Missense Mutation | CGT,TGT | R411C | NP_005826.1 |
| XM_005248784.2 | 1799 | Missense Mutation | ACG,ATG | T460M | XP_005248841.1 |
| XM_006714949.3 | 1799 | Missense Mutation | ACG,ATG | T460M | XP_006715012.1 |
| XM_006714950.2 | 1799 | Missense Mutation | ACG,ATG | T437M | XP_006715013.1 |
| XM_006714951.1 | 1799 | UTR 3 | XP_006715014.1 | ||
| XM_017010159.1 | 1799 | Missense Mutation | ACG,ATG | T437M | XP_016865648.1 |
| XM_017010160.1 | 1799 | UTR 3 | XP_016865649.1 |