| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_031308.3 | 15452 | Missense Mutation | CAG,CTG | Q5070L | NP_112598.3 |
| XM_017013889.1 | 15452 | Missense Mutation | CAG,CTG | Q5103L | XP_016869378.1 |
| XM_017013890.1 | 15452 | Missense Mutation | CAG,CTG | Q5070L | XP_016869379.1 |
| XM_017013891.1 | 15452 | Missense Mutation | CAG,CTG | Q4142L | XP_016869380.1 |
| XM_017013892.1 | 15452 | Missense Mutation | CAG,CTG | Q4036L | XP_016869381.1 |