| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282944.1 | 269 | Intron | NP_001269873.1 | ||
| NM_001282946.1 | 269 | Intron | NP_001269875.1 | ||
| NM_015160.2 | 269 | Intron | NP_055975.1 | ||
| XM_005266059.4 | 269 | Missense Mutation | CAC,CAG | H86Q | XP_005266116.1 |
| XM_011518417.2 | 269 | Intron | XP_011516719.1 | ||
| XM_017014543.1 | 269 | Intron | XP_016870032.1 |