| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080453.2 | 6349 | Missense Mutation | TGC,TTC | C2083F | NP_001073922.2 |
| XM_011515260.1 | 6349 | Missense Mutation | TGC,TTC | C2093F | XP_011513562.1 |
| XM_011515262.2 | 6349 | Intron | XP_011513564.1 | ||
| XM_017011959.1 | 6349 | Missense Mutation | TGC,TTC | C2093F | XP_016867448.1 |
| XM_017011960.1 | 6349 | Missense Mutation | TGC,TTC | C2083F | XP_016867449.1 |