| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159927.1 | 216 | Missense Mutation | CCT,CTT | P6L | NP_001153399.1 |
| NM_001159929.1 | 216 | Intron | NP_001153401.1 | ||
| NM_207102.2 | 216 | Missense Mutation | CCT,CTT | P6L | NP_996985.2 |
| XM_017006224.1 | 216 | Missense Mutation | CCT,CTT | P6L | XP_016861713.1 |