| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010906.1 | 1276 | Missense Mutation | ACG,GCG | T768A | NP_001010906.1 |
| XM_011544523.2 | 1276 | Intron | XP_011542825.1 | ||
| XM_011544524.2 | 1276 | Intron | XP_011542826.1 | ||
| XM_011544525.1 | 1276 | Missense Mutation | ACG,GCG | T381A | XP_011542827.1 |
| XM_011544526.2 | 1276 | Intron | XP_011542828.1 | ||
| XM_017013403.1 | 1276 | Intron | XP_016868892.1 |