| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001134999.1 | 2042 | Missense Mutation | CAC,CAG | H579Q | NP_001128471.1 |
| NM_001135000.1 | 2042 | Missense Mutation | CAC,CAG | H579Q | NP_001128472.1 |
| NM_006832.2 | 2042 | Missense Mutation | CAC,CAG | H572Q | NP_006823.1 |
| XM_005267285.2 | 2042 | Missense Mutation | CAC,CAG | H583Q | XP_005267342.1 |
| XM_006720008.2 | 2042 | Missense Mutation | CAC,CAG | H598Q | XP_006720071.1 |
| XM_006720009.2 | 2042 | Missense Mutation | CAC,CAG | H590Q | XP_006720072.1 |
| XM_006720010.2 | 2042 | Missense Mutation | CAC,CAG | H587Q | XP_006720073.1 |