| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199155.1 | 744 | Missense Mutation | CAG,CAT | Q176H | NP_001186084.1 |
| NM_001199156.1 | 744 | Intron | NP_001186085.1 | ||
| NM_001199157.1 | 744 | Intron | NP_001186086.1 | ||
| NM_001199158.1 | 744 | Intron | NP_001186087.1 | ||
| NM_007067.4 | 744 | Missense Mutation | CAG,CAT | Q176H | NP_008998.1 |
| XM_011524235.2 | 744 | Intron | XP_011522537.1 |