| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321825.1 | 2399 | Missense Mutation | CAT,CGT | H684R | NP_001308754.1 |
| NM_018086.3 | 2399 | Missense Mutation | CAT,CGT | H695R | NP_060556.2 |
| XM_011511389.2 | 2399 | Missense Mutation | CAT,CGT | H721R | XP_011509691.1 |
| XM_017004419.1 | 2399 | Missense Mutation | CAT,CGT | H721R | XP_016859908.1 |