| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000839.3 | 752 | Missense Mutation | CCG,CTG | P12L | NP_000830.2 |
| NM_001130063.1 | 752 | Intron | NP_001123535.1 | ||
| XM_011533635.1 | 752 | Missense Mutation | CCG,CTG | P12L | XP_011531937.1 |
| XM_011533636.1 | 752 | Missense Mutation | CCG,CTG | P12L | XP_011531938.1 |
| XM_011533637.1 | 752 | Intron | XP_011531939.1 | ||
| XM_011533638.2 | 752 | Intron | XP_011531940.1 | ||
| XM_011533639.2 | 752 | Intron | XP_011531941.1 | ||
| XM_011533640.2 | 752 | Intron | XP_011531942.1 | ||
| XM_011533641.2 | 752 | Intron | XP_011531943.1 | ||
| XM_011533642.1 | 752 | Missense Mutation | CCG,CTG | P12L | XP_011531944.1 |
| XM_011533643.1 | 752 | Intron | XP_011531945.1 | ||
| XM_011533644.1 | 752 | Intron | XP_011531946.1 | ||
| XM_011533645.1 | 752 | Intron | XP_011531947.1 | ||
| XM_011533646.2 | 752 | Intron | XP_011531948.1 | ||
| XM_011533647.1 | 752 | Intron | XP_011531949.1 | ||
| XM_017006271.1 | 752 | Missense Mutation | CCG,CTG | P12L | XP_016861760.1 |