| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003825.3 | 472 | Missense Mutation | AAT,GAT | N2D | NP_003816.2 |
| NM_130798.2 | 472 | Missense Mutation | AAT,GAT | N2D | NP_570710.1 |
| XM_006720725.2 | 472 | Missense Mutation | AAT,GAT | N2D | XP_006720788.1 |
| XM_017022692.1 | 472 | Missense Mutation | AAT,GAT | N2D | XP_016878181.1 |
| XM_017022693.1 | 472 | Intron | XP_016878182.1 | ||
| XM_017022694.1 | 472 | Intron | XP_016878183.1 |