| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252507.2 | 290 | Intron | NP_001239436.1 | ||
| NM_001282463.1 | 290 | Missense Mutation | TGG,TTG | W14L | NP_001269392.1 |
| NM_001282464.1 | 290 | Intron | NP_001269393.1 | ||
| NM_001289139.1 | 290 | Intron | NP_001276068.1 | ||
| XM_017021469.1 | 290 | Missense Mutation | TGG,TTG | W14L | XP_016876958.1 |