| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001007246.2 | 7192 | Intron | NP_001007247.1 | ||
| NM_018963.4 | 7192 | Silent Mutation | CTA,CTG | L2299L | NP_061836.2 |
| NM_033656.3 | 7192 | UTR 3 | NP_387505.1 | ||
| XM_011529611.1 | 7192 | Silent Mutation | CTA,CTG | L2251L | XP_011527913.1 |
| XM_011529612.2 | 7192 | Silent Mutation | CTA,CTG | L2019L | XP_011527914.1 |
| XM_011529613.1 | 7192 | Silent Mutation | CTA,CTG | L1310L | XP_011527915.1 |
| XM_017028373.1 | 7192 | Silent Mutation | CTA,CTG | L2212L | XP_016883862.1 |
| XM_017028374.1 | 7192 | Silent Mutation | CTA,CTG | L1310L | XP_016883863.1 |
| XM_017028375.1 | 7192 | Intron | XP_016883864.1 |