| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304448.1 | 773 | Missense Mutation | CTG,GTG | L106V | NP_001291377.1 |
| NM_002259.4 | 773 | Missense Mutation | CTG,GTG | L106V | NP_002250.1 |
| NM_007328.3 | 773 | Intron | NP_015567.1 | ||
| NM_213657.2 | 773 | Intron | NP_998822.1 | ||
| NM_213658.2 | 773 | Missense Mutation | CTG,GTG | L106V | NP_998823.1 |