| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006493.2 | 426 | Missense Mutation | CCA,CTA | P133L | NP_006484.1 |
| XM_011534917.2 | 426 | Missense Mutation | CCA,CTA | P133L | XP_011533219.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012158.2 | 426 | Intron | NP_036290.1 | ||
| XM_005266336.1 | 426 | Intron | XP_005266393.1 | ||
| XM_005266337.2 | 426 | Intron | XP_005266394.1 | ||
| XM_017020538.1 | 426 | Intron | XP_016876027.1 |