| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_033343.3 | 269 | Missense Mutation | ATC,GTC | I13V | NP_203129.1 |
| XM_011510105.2 | 269 | Intron | XP_011508407.1 | ||
| XM_011510106.2 | 269 | Intron | XP_011508408.1 | ||
| XM_011510108.2 | 269 | Intron | XP_011508410.1 | ||
| XM_017002755.1 | 269 | Intron | XP_016858244.1 |