| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000965.4 | 5490 | Intron | NP_000956.2 | ||
| NM_001290216.2 | 5490 | Intron | NP_001277145.1 | ||
| NM_001290217.1 | 5490 | Intron | NP_001277146.1 | ||
| NM_001290266.1 | 5490 | Intron | NP_001277195.1 | ||
| NM_001290276.1 | 5490 | Intron | NP_001277205.1 | ||
| NM_001290277.1 | 5490 | Intron | NP_001277206.1 | ||
| NM_001290300.1 | 5490 | Intron | NP_001277229.1 | ||
| NM_016152.3 | 5490 | Intron | NP_057236.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001068.3 | 5490 | Missense Mutation | GAA,GAT | E1612D | NP_001059.2 |
| XM_005265427.3 | 5490 | Missense Mutation | GAA,GAT | E1617D | XP_005265484.1 |
| XM_011534057.2 | 5490 | Missense Mutation | GAA,GAT | E1580D | XP_011532359.1 |