| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015114.2 | 2099 | Missense Mutation | CCG,CTG | P897L | NP_055929.1 |
| XM_005266159.3 | 2099 | Missense Mutation | CCG,CTG | P835L | XP_005266216.1 |
| XM_005266160.1 | 2099 | Missense Mutation | CCG,CTG | P835L | XP_005266217.1 |
| XM_006719735.1 | 2099 | UTR 3 | XP_006719798.1 | ||
| XM_011534787.2 | 2099 | Intron | XP_011533089.1 | ||
| XM_011534788.1 | 2099 | Intron | XP_011533090.1 | ||
| XM_017019076.1 | 2099 | Missense Mutation | CCG,CTG | P460L | XP_016874565.1 |