| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001307930.1 | 658 | Intron | NP_001294859.1 | ||
| NM_016563.3 | 658 | Intron | NP_057647.1 | ||
| XM_005254434.4 | 658 | Intron | XP_005254491.1 | ||
| XM_011521660.2 | 658 | Intron | XP_011519962.1 | ||
| XM_017022296.1 | 658 | Intron | XP_016877785.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178859.3 | 658 | Missense Mutation | CCG,CTG | P121L | NP_849190.2 |
| XM_005254159.4 | 658 | Missense Mutation | CCG,CTG | P121L | XP_005254216.1 |