| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001205201.1 | 47 | Intron | NP_001192130.1 | ||
| NM_001586.2 | 47 | Intron | NP_001577.1 | ||
| XM_011531116.1 | 47 | Missense Mutation | GCG,GTG | A10V | XP_011529418.1 |
| XM_011531117.1 | 47 | Intron | XP_011529419.1 | ||
| XM_011531118.2 | 47 | Intron | XP_011529420.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145933.1 | 47 | Intron | NP_001139405.1 | ||
| NM_001145934.1 | 47 | Intron | NP_001139406.1 | ||
| NM_012253.3 | 47 | Intron | NP_036385.3 |