| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012274.1 | 42 | Missense Mutation | GGT,TGT | G7C | NP_036406.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163334.1 | 42 | Intron | NP_001156806.1 | ||
| NM_001163335.1 | 42 | Intron | NP_001156807.1 | ||
| NM_138780.2 | 42 | Intron | NP_620135.1 | ||
| XM_011544001.2 | 42 | Intron | XP_011542303.1 | ||
| XM_011544002.2 | 42 | Intron | XP_011542304.1 | ||
| XM_017029972.1 | 42 | Intron | XP_016885461.1 | ||
| XM_017029973.1 | 42 | Intron | XP_016885462.1 | ||
| XM_017029974.1 | 42 | Intron | XP_016885463.1 |