| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001306153.1 | 496 | Missense Mutation | AAT,GAT | N61D | NP_001293082.1 |
| NM_001306154.1 | 496 | Intron | NP_001293083.1 | ||
| NM_001306155.1 | 496 | Intron | NP_001293084.1 | ||
| NM_001306156.1 | 496 | Missense Mutation | AAT,GAT | N44D | NP_001293085.1 |
| NM_012073.4 | 496 | Missense Mutation | AAT,GAT | N82D | NP_036205.1 |