| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282415.1 | 2052 | Missense Mutation | CTG,GTG | L315V | NP_001269344.1 |
| NM_001282416.1 | 2052 | Missense Mutation | CTG,GTG | L572V | NP_001269345.1 |
| NM_032805.2 | 2052 | Missense Mutation | CTG,GTG | L709V | NP_116194.2 |
| XM_017023791.1 | 2052 | Missense Mutation | CTG,GTG | L709V | XP_016879280.1 |
| XM_017023792.1 | 2052 | Missense Mutation | CTG,GTG | L677V | XP_016879281.1 |