| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167903.1 | 389 | Silent Mutation | CTA,CTG | L112L | NP_001161375.1 |
| NM_001289406.1 | 389 | Silent Mutation | CTA,CTG | L5L | NP_001276335.1 |
| NM_001289407.1 | 389 | UTR 5 | NP_001276336.1 | ||
| NM_022736.2 | 389 | Missense Mutation | ACC,GCC | T114A | NP_073573.2 |
| XM_006713730.2 | 389 | Silent Mutation | CTA,CTG | L112L | XP_006713793.1 |