| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318204.1 | 1725 | Intron | NP_001305133.1 | ||
| NM_004560.3 | 1725 | Missense Mutation | CAC,CAG | H940Q | NP_004551.2 |
| XM_005252008.4 | 1725 | Missense Mutation | CAC,CAG | H800Q | XP_005252065.1 |
| XM_005252009.3 | 1725 | Missense Mutation | CAC,CAG | H539Q | XP_005252066.1 |
| XM_006717121.3 | 1725 | Missense Mutation | CAC,CAG | H800Q | XP_006717184.1 |
| XM_017014762.1 | 1725 | Missense Mutation | CAC,CAG | H937Q | XP_016870251.1 |
| XM_017014763.1 | 1725 | Missense Mutation | CAC,CAG | H800Q | XP_016870252.1 |