| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008225.2 | 2299 | Intron | NP_001008226.1 | ||
| NM_001190847.1 | 2299 | Missense Mutation | CAC,CAG | H585Q | NP_001177776.1 |
| NM_001190848.1 | 2299 | Intron | NP_001177777.1 | ||
| NM_001190849.1 | 2299 | Missense Mutation | CAC,CAG | H653Q | NP_001177778.1 |
| NM_001190850.1 | 2299 | Missense Mutation | CAC,CAG | H656Q | NP_001177779.1 |
| NM_013316.3 | 2299 | Missense Mutation | CAC,CAG | H582Q | NP_037448.2 |
| XM_017012235.1 | 2299 | Missense Mutation | CAC,CAG | H656Q | XP_016867724.1 |