| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256113.1 | 1099 | Intron | NP_001243042.1 | ||
| NM_175075.4 | 1099 | Missense Mutation | CTG,GTG | L177V | NP_778250.2 |
| XM_006716232.3 | 1099 | Missense Mutation | CTG,GTG | L177V | XP_006716295.1 |
| XM_017013113.1 | 1099 | Missense Mutation | CTG,GTG | L187V | XP_016868602.1 |