| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271842.1 | 416 | Missense Mutation | CAC,CCC | H97P | NP_001258771.1 |
| NM_001319190.1 | 416 | Intron | NP_001306119.1 | ||
| NM_207103.3 | 416 | Missense Mutation | CAC,CCC | H104P | NP_996986.1 |
| XM_017024615.1 | 416 | Intron | XP_016880104.1 |