| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271842.1 | 502 | Missense Mutation | AAT,GAT | N126D | NP_001258771.1 |
| NM_001319190.1 | 502 | Intron | NP_001306119.1 | ||
| NM_207103.3 | 502 | Missense Mutation | AAT,GAT | N133D | NP_996986.1 |
| XM_017024615.1 | 502 | Intron | XP_016880104.1 |