| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_144719.3 | 1603 | Silent Mutation | CTA,CTG | L707L | NP_653320.3 |
| XM_005264898.3 | 1603 | Silent Mutation | CTA,CTG | L666L | XP_005264955.1 |
| XM_005264899.4 | 1603 | Intron | XP_005264956.1 | ||
| XM_011533418.2 | 1603 | Silent Mutation | CTA,CTG | L638L | XP_011531720.1 |
| XM_011533419.2 | 1603 | Silent Mutation | CTA,CTG | L487L | XP_011531721.1 |
| XM_011533420.2 | 1603 | Intron | XP_011531722.1 | ||
| XM_011533421.2 | 1603 | Intron | XP_011531723.1 | ||
| XM_017005781.1 | 1603 | Silent Mutation | CTA,CTG | L487L | XP_016861270.1 |