| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278201.1 | 1617 | Missense Mutation | CTG,GTG | L429V | NP_001265130.1 |
| NM_001278206.1 | 1617 | Missense Mutation | CTG,GTG | L442V | NP_001265135.1 |
| NM_014096.3 | 1617 | Missense Mutation | CTG,GTG | L429V | NP_054815.2 |
| NM_017611.2 | 1617 | Missense Mutation | CTG,GTG | L429V | NP_060081.1 |
| NM_199329.2 | 1617 | Missense Mutation | CTG,GTG | L429V | NP_955361.1 |