| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199461.1 | 806 | Intron | NP_001186390.1 | ||
| NM_001199462.1 | 806 | Missense Mutation | AAA,ACA | K199T | NP_001186391.1 |
| NM_001199463.1 | 806 | Intron | NP_001186392.1 | ||
| NM_001199464.1 | 806 | Intron | NP_001186393.1 | ||
| NM_002598.3 | 806 | Missense Mutation | AAA,ACA | K232T | NP_002589.2 |
| NM_144781.2 | 806 | Intron | NP_659005.1 | ||
| XM_017010926.1 | 806 | Missense Mutation | AAA,ACA | K232T | XP_016866415.1 |