| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016453.3 | 2133 | Silent Mutation | CTG,TTG | L663L | NP_057537.1 |
| NM_184231.2 | 2133 | Silent Mutation | CTG,TTG | L656L | NP_909119.1 |
| XM_017006594.1 | 2133 | Intron | XP_016862083.1 | ||
| XM_017006595.1 | 2133 | Intron | XP_016862084.1 | ||
| XM_017006596.1 | 2133 | Intron | XP_016862085.1 | ||
| XM_017006597.1 | 2133 | Intron | XP_016862086.1 | ||
| XM_017006598.1 | 2133 | Intron | XP_016862087.1 | ||
| XM_017006599.1 | 2133 | Silent Mutation | CTG,TTG | L585L | XP_016862088.1 |
| XM_017006600.1 | 2133 | Silent Mutation | CTG,TTG | L578L | XP_016862089.1 |