| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130674.2 | 988 | UTR 3 | NP_001124146.1 | ||
| NM_001199671.1 | 988 | UTR 3 | NP_001186600.1 | ||
| NM_001199672.1 | 988 | UTR 3 | NP_001186601.1 | ||
| NM_001199673.1 | 988 | UTR 3 | NP_001186602.1 | ||
| NM_001219.4 | 988 | UTR 3 | NP_001210.1 | ||
| XM_017012659.1 | 988 | Intron | XP_016868148.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001708.2 | 988 | Missense Mutation | AGC,TGC | S330C | NP_001699.1 |