| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001791.2 | 669 | Missense Mutation | AGC,GGC | S110G | NP_001001791.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145031.2 | 669 | UTR 5 | NP_001138503.1 | ||
| NM_001319191.1 | 669 | Intron | NP_001306120.1 | ||
| NM_002658.4 | 669 | Intron | NP_002649.1 | ||
| XM_011539866.2 | 669 | Intron | XP_011538168.1 |