| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256538.1 | 208 | Missense Mutation | CGT,TGT | R12C | NP_001243467.1 |
| NM_080739.2 | 208 | Missense Mutation | CGT,TGT | R12C | NP_542777.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167670.2 | 208 | Intron | NP_001161142.1 | ||
| NM_001318207.1 | 208 | Intron | NP_001305136.1 | ||
| XM_011529128.2 | 208 | Intron | XP_011527430.1 | ||
| XM_011529129.2 | 208 | Intron | XP_011527431.1 |