| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010879.3 | 475 | Missense Mutation | AAT,GAT | N45D | NP_001010879.2 |
| NM_001321145.1 | 475 | Missense Mutation | AAT,GAT | N32D | NP_001308074.1 |
| NM_001321146.1 | 475 | UTR 5 | NP_001308075.1 | ||
| NM_001321147.1 | 475 | Intron | NP_001308076.1 | ||
| XM_011526761.1 | 475 | Missense Mutation | AAT,GAT | N31D | XP_011525063.1 |
| XM_011526762.1 | 475 | Missense Mutation | AAT,GAT | N26D | XP_011525064.1 |
| XM_011526763.1 | 475 | Missense Mutation | AAT,GAT | N18D | XP_011525065.1 |
| XM_011526764.1 | 475 | Missense Mutation | AAT,GAT | N12D | XP_011525066.1 |
| XM_011526765.2 | 475 | Intron | XP_011525067.1 | ||
| XM_011526766.2 | 475 | UTR 5 | XP_011525068.1 | ||
| XM_011526767.2 | 475 | Intron | XP_011525069.1 |