| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006844.4 | 1702 | Missense Mutation | NP_006835.2 | ||
| XM_005259717.4 | 1702 | Missense Mutation | XP_005259774.1 | ||
| XM_011527651.2 | 1702 | Missense Mutation | XP_011525953.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300910.1 | 1702 | Intron | NP_001287839.1 | ||
| NM_033025.5 | 1702 | Intron | NP_149014.3 |