| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022772.3 | 388 | Silent Mutation | CAC,CAT | H47H | NP_073609.2 |
| XM_017018130.1 | 388 | Missense Mutation | CAC,CAT | H47H | XP_016873619.1 |
| XM_017018131.1 | 388 | Missense Mutation | CAC,CAT | H47H | XP_016873620.1 |
| XM_017018132.1 | 388 | Missense Mutation | CAC,CAT | H47H | XP_016873621.1 |