| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321307.1 | 5000 | Missense Mutation | CAT,CGT | H1385R | NP_001308236.1 |
| NM_002519.2 | 5000 | Missense Mutation | CAT,CGT | H1378R | NP_002510.2 |
| XM_011542854.2 | 5000 | Missense Mutation | CAT,CGT | H1387R | XP_011541156.1 |
| XM_017017802.1 | 5000 | Missense Mutation | CAT,CGT | H1319R | XP_016873291.1 |
| XM_017017803.1 | 5000 | Missense Mutation | CAT,CGT | H1319R | XP_016873292.1 |