| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001290553.1 | 997 | Intron | NP_001277482.1 | ||
| NM_001290557.1 | 997 | Missense Mutation | CCC,TCC | P231S | NP_001277486.1 |
| NM_001290629.1 | 997 | Intron | NP_001277558.1 | ||
| NM_015999.5 | 997 | Missense Mutation | CCC,TCC | P231S | NP_057083.2 |
| XM_017001407.1 | 997 | Intron | XP_016856896.1 |