| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039583.1 | 71 | Missense Mutation | CAC,CAG | H30Q | NP_001034672.1 |
| NM_001039584.1 | 71 | Missense Mutation | CAC,CAG | H30Q | NP_001034673.1 |
| NM_012407.3 | 71 | Missense Mutation | CAC,CAG | H30Q | NP_036539.1 |
| XM_006724379.2 | 71 | UTR 5 | XP_006724442.1 | ||
| XM_006724380.2 | 71 | UTR 5 | XP_006724443.1 | ||
| XM_011530517.2 | 71 | Missense Mutation | CAC,CAG | H30Q | XP_011528819.1 |
| XM_017029090.1 | 71 | Intron | XP_016884579.1 | ||
| XM_017029091.1 | 71 | Intron | XP_016884580.1 | ||
| XM_017029092.1 | 71 | UTR 5 | XP_016884581.1 | ||
| XM_017029093.1 | 71 | Intron | XP_016884582.1 | ||
| XM_017029094.1 | 71 | Intron | XP_016884583.1 | ||
| XM_017029095.1 | 71 | UTR 5 | XP_016884584.1 |