| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286496.1 | 1919 | Missense Mutation | AAT,GAT | N626D | NP_001273425.1 |
| NM_001286497.1 | 1919 | Intron | NP_001273426.1 | ||
| NM_001286499.1 | 1919 | Missense Mutation | AAT,GAT | N573D | NP_001273428.1 |
| NM_025049.3 | 1919 | Missense Mutation | AAT,GAT | N626D | NP_079325.2 |
| XM_011522083.2 | 1919 | Missense Mutation | AAT,GAT | N626D | XP_011520385.1 |
| XM_011522084.2 | 1919 | Missense Mutation | AAT,GAT | N626D | XP_011520386.1 |