| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006369.4 | 2316 | Missense Mutation | CGC,TGC | R758C | NP_006360.3 |
| XM_017000074.1 | 2316 | Intron | XP_016855563.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142548.1 | 2316 | Intron | NP_001136020.1 | ||
| NM_003579.3 | 2316 | Intron | NP_003570.2 | ||
| XM_006710975.3 | 2316 | Intron | XP_006711038.1 | ||
| XM_011542299.2 | 2316 | Intron | XP_011540601.1 | ||
| XM_011542300.2 | 2316 | Intron | XP_011540602.1 |