| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024746.3 | 1821 | Intron | NP_079022.2 | ||
| XM_011509985.2 | 1821 | Intron | XP_011508287.1 | ||
| XM_011509986.1 | 1821 | Missense Mutation | CAG,CAT | Q606H | XP_011508288.1 |
| XM_017002350.1 | 1821 | Intron | XP_016857839.1 |