| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001220484.1 | 3748 | Missense Mutation | CAT,CGT | H973R | NP_001207413.1 |
| NM_203309.2 | 3748 | Missense Mutation | CAT,CGT | H973R | NP_976054.2 |
| XM_006720143.2 | 3748 | Missense Mutation | CAT,CGT | H973R | XP_006720206.1 |
| XM_011536760.2 | 3748 | Missense Mutation | CAT,CGT | H973R | XP_011535062.1 |
| XM_011536761.2 | 3748 | Intron | XP_011535063.1 | ||
| XM_017021289.1 | 3748 | Missense Mutation | CAT,CGT | H973R | XP_016876778.1 |