| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164741.1 | 2907 | Missense Mutation | CCG,CTG | P950L | NP_001158213.1 |
| NM_001666.4 | 2907 | Missense Mutation | CCG,CTG | P910L | NP_001657.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000054.4 | 2907 | Intron | NP_000045.1 | ||
| NM_001146151.1 | 2907 | Intron | NP_001139623.1 | ||
| XM_006724828.3 | 2907 | Intron | XP_006724891.1 |