| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303486.1 | 3208 | Missense Mutation | CAT,CCT | H887P | NP_001290415.1 |
| NM_001303487.1 | 3208 | Missense Mutation | CAT,CCT | H861P | NP_001290416.1 |
| NM_001303489.1 | 3208 | Missense Mutation | CAT,CCT | H555P | NP_001290418.1 |
| NM_001324381.1 | 3208 | Missense Mutation | CAT,CCT | H887P | NP_001311310.1 |
| NM_003631.3 | 3208 | Missense Mutation | CAT,CCT | H969P | NP_003622.2 |
| XM_011540305.1 | 3208 | Missense Mutation | CAT,CCT | H928P | XP_011538607.1 |
| XM_011540308.2 | 3208 | Intron | XP_011538610.1 |