| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017560.1 | 1048 | Missense Mutation | CTG,GTG | L203V | NP_060030.1 |
| XM_011515438.2 | 1048 | Missense Mutation | CTG,GTG | L229V | XP_011513740.1 |
| XM_011515439.2 | 1048 | Missense Mutation | CTG,GTG | L214V | XP_011513741.1 |
| XM_017012371.1 | 1048 | Missense Mutation | CTG,GTG | L188V | XP_016867860.1 |