| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282750.1 | 189 | Intron | NP_001269679.1 | ||
| NM_001282751.1 | 189 | Intron | NP_001269680.1 | ||
| NM_014283.4 | 189 | Intron | NP_055098.1 | ||
| NM_016227.3 | 189 | Missense Mutation | CCA,CTA | P22L | NP_057311.3 |
| XM_006711374.2 | 189 | Intron | XP_006711437.1 | ||
| XM_006711375.2 | 189 | Intron | XP_006711438.1 | ||
| XM_006711376.1 | 189 | Intron | XP_006711439.1 |