| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317031.1 | 1572 | Missense Mutation | ACG,ATG | T171M | NP_001303960.1 |
| NM_001317032.1 | 1572 | Intron | NP_001303961.1 | ||
| NM_001317033.1 | 1572 | UTR 3 | NP_001303962.1 | ||
| NM_182513.3 | 1572 | UTR 3 | NP_872319.1 | ||
| XM_005259753.3 | 1572 | Intron | XP_005259810.1 | ||
| XM_011527702.1 | 1572 | UTR 3 | XP_011526004.1 |