| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321116.1 | 539 | Missense Mutation | CCG,CTG | P131L | NP_001308045.1 |
| NM_001321117.1 | 539 | Intron | NP_001308046.1 | ||
| NM_181846.2 | 539 | Missense Mutation | CCG,CTG | P131L | NP_862829.1 |
| XM_006723192.3 | 539 | Missense Mutation | CCG,CTG | P131L | XP_006723255.1 |
| XM_011526917.2 | 539 | Missense Mutation | CCG,CTG | P131L | XP_011525219.1 |
| XM_011526918.2 | 539 | Intron | XP_011525220.1 | ||
| XM_017026746.1 | 539 | Intron | XP_016882235.1 | ||
| XM_017026747.1 | 539 | Intron | XP_016882236.1 |