| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135163.1 | 1704 | Intron | NP_001128635.1 | ||
| NM_052884.2 | 1704 | Intron | NP_443116.2 | ||
| XM_005258476.3 | 1704 | Missense Mutation | ACT,GCT | T558A | XP_005258533.2 |
| XM_005258477.3 | 1704 | Intron | XP_005258534.2 |