| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001139443.1 | 657 | Intron | NP_001132915.1 | ||
| NM_001300786.1 | 657 | Intron | NP_001287715.1 | ||
| NM_001300787.1 | 657 | Intron | NP_001287716.1 | ||
| NM_004183.3 | 657 | Missense Mutation | GAC,GGC | D26G | NP_004174.1 |