| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286457.1 | 3961 | Intron | NP_001273386.1 | ||
| NM_001286458.1 | 3961 | Intron | NP_001273387.1 | ||
| NM_001321858.1 | 3961 | Intron | NP_001308787.1 | ||
| NM_003470.2 | 3961 | Intron | NP_003461.2 | ||
| XM_017023652.1 | 3961 | Missense Mutation | AAG,GAG | K1112E | XP_016879141.1 |
| XM_017023653.1 | 3961 | Missense Mutation | AAG,GAG | K1096E | XP_016879142.1 |