| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032184.1 | 2942 | Missense Mutation | GAT,GTT | D1169V | NP_115560.1 |
| XM_005271254.3 | 2942 | Intron | XP_005271311.1 | ||
| XM_006710946.3 | 2942 | Intron | XP_006711009.1 | ||
| XM_017002483.1 | 2942 | Intron | XP_016857972.1 | ||
| XM_017002484.1 | 2942 | Intron | XP_016857973.1 | ||
| XM_017002485.1 | 2942 | Missense Mutation | GAT,GTT | D911V | XP_016857974.1 |
| XM_017002486.1 | 2942 | Missense Mutation | GAT,GTT | D911V | XP_016857975.1 |