| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286379.1 | 132 | Intron | NP_001273308.1 | ||
| NM_001286380.1 | 132 | Missense Mutation | GAG,GTG | E16V | NP_001273309.1 |
| NM_001286381.1 | 132 | Intron | NP_001273310.1 | ||
| NM_032448.2 | 132 | Intron | NP_115824.1 | ||
| XM_011536185.2 | 132 | Intron | XP_011534487.1 | ||
| XM_017011357.1 | 132 | Intron | XP_016866846.1 | ||
| XM_017011358.1 | 132 | Intron | XP_016866847.1 | ||
| XM_017011359.1 | 132 | Intron | XP_016866848.1 | ||
| XM_017011360.1 | 132 | Intron | XP_016866849.1 |