| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001026.4 | 189 | Intron | NP_001017.1 | ||
| NM_001142282.1 | 189 | Intron | NP_001135754.1 | ||
| NM_001142283.1 | 189 | Intron | NP_001135755.1 | ||
| NM_001142284.1 | 189 | Intron | NP_001135756.1 | ||
| NM_001142285.1 | 189 | Missense Mutation | CGA,CTA | R16L | NP_001135757.1 |
| NM_033022.3 | 189 | Intron | NP_148982.1 |