| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000288.3 | 562 | Missense Mutation | CAC,CCC | H39P | NP_000279.1 |
| XM_005267019.4 | 562 | Intron | XP_005267076.1 | ||
| XM_006715502.1 | 562 | Missense Mutation | CAC,CCC | H39P | XP_006715565.1 |
| XM_017010934.1 | 562 | Missense Mutation | CAC,CCC | H39P | XP_016866423.1 |