| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001316963.1 | 660 | Missense Mutation | CAT,CGT | H100R | NP_001303892.1 |
| NM_001729.3 | 660 | Missense Mutation | CAT,CGT | H149R | NP_001720.1 |
| XM_011532211.1 | 660 | Missense Mutation | CAT,CGT | H149R | XP_011530513.1 |
| XM_017008568.1 | 660 | Intron | XP_016864057.1 |