| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308120.1 | 235 | Missense Mutation | CCG,CTG | P11L | NP_001295049.1 |
| NM_015091.3 | 235 | Missense Mutation | CCG,CTG | P11L | NP_055906.2 |
| XM_011536571.1 | 235 | Missense Mutation | CCG,CTG | P11L | XP_011534873.1 |
| XM_017021098.1 | 235 | Missense Mutation | CCG,CTG | P11L | XP_016876587.1 |
| XM_017021099.1 | 235 | Missense Mutation | CCG,CTG | P11L | XP_016876588.1 |
| XM_017021100.1 | 235 | Missense Mutation | CCG,CTG | P11L | XP_016876589.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308112.1 | 235 | Intron | NP_001295041.1 | ||
| NM_017658.4 | 235 | Intron | NP_060128.2 | ||
| XM_005267770.3 | 235 | Intron | XP_005267827.1 | ||
| XM_006720174.3 | 235 | Intron | XP_006720237.1 | ||
| XM_011536847.2 | 235 | Intron | XP_011535149.1 | ||
| XM_011536849.2 | 235 | Intron | XP_011535151.1 | ||
| XM_017021378.1 | 235 | Intron | XP_016876867.1 |