| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000536.3 | 1596 | Missense Mutation | CCC,CTC | P464L | NP_000527.2 |
| NM_001243785.1 | 1596 | Missense Mutation | CCC,CTC | P464L | NP_001230714.1 |
| NM_001243786.1 | 1596 | Missense Mutation | CCC,CTC | P464L | NP_001230715.1 |