| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152542.4 | 582 | Missense Mutation | CAG,CAT | Q286H | NP_689755.3 |
| XM_005262775.3 | 582 | Intron | XP_005262832.1 | ||
| XM_006714111.3 | 582 | Missense Mutation | CAG,CAT | Q286H | XP_006714174.1 |
| XM_017007803.1 | 582 | Missense Mutation | CAG,CAT | Q286H | XP_016863292.1 |
| XM_017007804.1 | 582 | Missense Mutation | CAG,CAT | Q177H | XP_016863293.1 |
| XM_017007805.1 | 582 | Missense Mutation | CAG,CAT | Q177H | XP_016863294.1 |
| XM_017007806.1 | 582 | Missense Mutation | CAG,CAT | Q177H | XP_016863295.1 |
| XM_017007807.1 | 582 | Missense Mutation | CAG,CAT | Q158H | XP_016863296.1 |