| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171815.1 | 708 | Silent Mutation | CTC,CTG | L123L | NP_001165286.1 |
| NM_001171816.1 | 708 | Silent Mutation | CTC,CTG | L95L | NP_001165287.1 |
| NM_178841.3 | 708 | Silent Mutation | CTC,CTG | L204L | NP_849163.1 |
| XM_011522845.2 | 708 | Missense Mutation | CCT,GCT | P257A | XP_011521147.1 |
| XM_011522846.1 | 708 | Silent Mutation | CTC,CTG | L204L | XP_011521148.1 |
| XM_011522847.1 | 708 | Silent Mutation | CTC,CTG | L95L | XP_011521149.1 |
| XM_017022910.1 | 708 | Missense Mutation | CCT,GCT | P283A | XP_016878399.1 |
| XM_017022911.1 | 708 | Intron | XP_016878400.1 | ||
| XM_017022912.1 | 708 | Intron | XP_016878401.1 | ||
| XM_017022913.1 | 708 | Silent Mutation | CTC,CTG | L95L | XP_016878402.1 |