| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001002857.1 | 1046 | Intron | NP_001002857.1 | ||
| NM_001002858.2 | 1046 | Missense Mutation | CTC,TTC | L325F | NP_001002858.1 |
| NM_001136015.2 | 1046 | Intron | NP_001129487.1 | ||
| NM_004039.2 | 1046 | Intron | NP_004030.1 | ||
| XM_011521477.2 | 1046 | Intron | XP_011519779.1 | ||
| XM_017022090.1 | 1046 | Intron | XP_016877579.1 | ||
| XM_017022091.1 | 1046 | Intron | XP_016877580.1 | ||
| XM_017022092.1 | 1046 | Intron | XP_016877581.1 | ||
| XM_017022093.1 | 1046 | Intron | XP_016877582.1 |