| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_031308.3 | 15439 | Missense Mutation | CTG,GTG | L5066V | NP_112598.3 |
| XM_017013889.1 | 15439 | Missense Mutation | CTG,GTG | L5099V | XP_016869378.1 |
| XM_017013890.1 | 15439 | Missense Mutation | CTG,GTG | L5066V | XP_016869379.1 |
| XM_017013891.1 | 15439 | Missense Mutation | CTG,GTG | L4138V | XP_016869380.1 |
| XM_017013892.1 | 15439 | Missense Mutation | CTG,GTG | L4032V | XP_016869381.1 |