| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243998.1 | 196 | Intron | NP_001230927.1 | ||
| NM_001243999.1 | 196 | Silent Mutation | CCC,CCT | P57P | NP_001230928.1 |
| NM_001244000.1 | 196 | Missense Mutation | CCT,CTT | P38L | NP_001230929.1 |
| NM_003121.4 | 196 | Silent Mutation | CCC,CCT | P57P | NP_003112.2 |