| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304334.1 | 519 | Missense Mutation | CCT,GCT | P98A | NP_001291263.1 |
| NM_001304335.1 | 519 | Intron | NP_001291264.1 | ||
| NM_001304336.1 | 519 | Silent Mutation | CTC,CTG | L96L | NP_001291265.1 |
| NM_001304337.1 | 519 | Intron | NP_001291266.1 | ||
| NM_198542.2 | 519 | Missense Mutation | CCT,GCT | P99A | NP_940944.1 |