| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135570.1 | 1119 | Intron | NP_001129042.1 | ||
| XM_011538718.2 | 1119 | Missense Mutation | CAG,CCG | Q107P | XP_011537020.1 |
| XM_017019916.1 | 1119 | Intron | XP_016875405.1 | ||
| XM_017019917.1 | 1119 | Intron | XP_016875406.1 |