| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_005260641.3 | 1494 | Missense Mutation | CAC,CTC | H370L | XP_005260698.1 |
| XM_005260643.3 | 1494 | Missense Mutation | CAC,CTC | H259L | XP_005260700.1 |
| XM_005260644.3 | 1494 | Missense Mutation | CAC,CTC | H153L | XP_005260701.1 |
| XM_011529130.2 | 1494 | Intron | XP_011527432.1 | ||
| XM_011529134.2 | 1494 | Intron | XP_011527436.1 | ||
| XM_017027577.1 | 1494 | Missense Mutation | CAC,CTC | H371L | XP_016883066.1 |
| XM_017027578.1 | 1494 | Intron | XP_016883067.1 | ||
| XM_017027579.1 | 1494 | Intron | XP_016883068.1 | ||
| XM_017027580.1 | 1494 | Intron | XP_016883069.1 | ||
| XM_017027581.1 | 1494 | Silent Mutation | ACA,ACT | T327T | XP_016883070.1 |
| XM_017027582.1 | 1494 | Silent Mutation | ACA,ACT | T327T | XP_016883071.1 |
| XM_017027583.1 | 1494 | Intron | XP_016883072.1 | ||
| XM_017027584.1 | 1494 | Intron | XP_016883073.1 | ||
| XM_017027585.1 | 1494 | Missense Mutation | CAC,CTC | H260L | XP_016883074.1 |