| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001004196.3 | 492 | Missense Mutation | ACA,GCA | T18A | NP_001004196.2 |
| NM_001318826.1 | 492 | Intron | NP_001305755.1 | ||
| NM_001318828.1 | 492 | Intron | NP_001305757.1 | ||
| NM_001318830.1 | 492 | Intron | NP_001305759.1 | ||
| NM_005944.6 | 492 | Intron | NP_005935.4 | ||
| XM_005247481.4 | 492 | Missense Mutation | ACA,GCA | T18A | XP_005247538.1 |
| XM_005247482.2 | 492 | Intron | XP_005247539.1 | ||
| XM_005247485.2 | 492 | Intron | XP_005247542.1 | ||
| XM_005247486.2 | 492 | Intron | XP_005247543.1 | ||
| XM_005247488.2 | 492 | Intron | XP_005247545.1 | ||
| XM_017006452.1 | 492 | UTR 5 | XP_016861941.1 | ||
| XM_017006453.1 | 492 | Intron | XP_016861942.1 | ||
| XM_017006454.1 | 492 | UTR 5 | XP_016861943.1 | ||
| XM_017006455.1 | 492 | Intron | XP_016861944.1 | ||
| XM_017006456.1 | 492 | UTR 5 | XP_016861945.1 | ||
| XM_017006457.1 | 492 | Intron | XP_016861946.1 | ||
| XM_017006458.1 | 492 | UTR 5 | XP_016861947.1 | ||
| XM_017006459.1 | 492 | Intron | XP_016861948.1 |