| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278237.1 | 452 | UTR 5 | NP_001265166.1 | ||
| NM_014254.2 | 452 | Missense Mutation | ACG,ATG | T92M | NP_055069.1 |
| XM_005268562.3 | 452 | UTR 5 | XP_005268619.1 | ||
| XM_005268563.3 | 452 | UTR 5 | XP_005268620.1 | ||
| XM_017018686.1 | 452 | UTR 5 | XP_016874175.1 | ||
| XM_017018687.1 | 452 | UTR 5 | XP_016874176.1 |