| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142314.1 | 497 | Missense Mutation | CAT,CGT | H41R | NP_001135786.1 |
| NM_001321519.1 | 497 | Missense Mutation | CAT,CGT | H41R | NP_001308448.1 |
| NM_080876.3 | 497 | Missense Mutation | CAT,CGT | H41R | NP_543152.1 |