| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172779.1 | 1229 | Missense Mutation | AAT,GAT | N421D | NP_001166250.1 |
| NM_001172780.1 | 1229 | Intron | NP_001166251.1 | ||
| NM_153353.4 | 1229 | Missense Mutation | AAT,GAT | N389D | NP_699184.2 |
| XM_006713508.3 | 1229 | Missense Mutation | AAT,GAT | N403D | XP_006713571.1 |
| XM_011512442.2 | 1229 | Missense Mutation | AAT,GAT | N420D | XP_011510744.1 |
| XM_017005746.1 | 1229 | Missense Mutation | AAT,GAT | N359D | XP_016861235.1 |