| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001128829.3 | 666 | Missense Mutation | CCT,CTT | P196L | NP_001122301.1 |
| NM_001128830.3 | 666 | Missense Mutation | CCT,CTT | P196L | NP_001122302.1 |
| NM_001128831.3 | 666 | Missense Mutation | CCT,CTT | P196L | NP_001122303.1 |
| NM_001164830.1 | 666 | Missense Mutation | CCT,CTT | P196L | NP_001158302.1 |
| NM_001291967.1 | 666 | Missense Mutation | CCT,CTT | P130L | NP_001278896.1 |
| NM_001291968.1 | 666 | Missense Mutation | CCT,CTT | P83L | NP_001278897.1 |
| NM_001738.4 | 666 | Missense Mutation | CCT,CTT | P196L | NP_001729.1 |