| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001525.2 | 954 | Intron | NP_001516.2 | ||
| XM_017001105.1 | 954 | Intron | XP_016856594.1 | ||
| XM_017001106.1 | 954 | Intron | XP_016856595.1 | ||
| XM_017001107.1 | 954 | Missense Mutation | CCG,CTG | P387L | XP_016856596.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012392.3 | 954 | Silent Mutation | ACA,ACG | T204T | NP_036524.1 |
| XM_011541745.1 | 954 | Silent Mutation | ACA,ACG | T199T | XP_011540047.1 |
| XM_011541746.2 | 954 | Silent Mutation | ACA,ACG | T134T | XP_011540048.1 |
| XM_011541747.1 | 954 | Silent Mutation | ACA,ACG | T134T | XP_011540049.1 |
| XM_017001680.1 | 954 | Silent Mutation | ACA,ACG | T134T | XP_016857169.1 |
| XM_017001681.1 | 954 | Intron | XP_016857170.1 |