| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001299.5 | 149 | Missense Mutation | CCG,CGG | P30R | NP_001290.2 |
| NM_001308341.1 | 149 | UTR 5 | NP_001295270.1 | ||
| NM_001308342.1 | 149 | UTR 5 | NP_001295271.1 | ||
| XM_005259741.2 | 149 | UTR 5 | XP_005259798.1 | ||
| XM_017026289.1 | 149 | Missense Mutation | CCG,CGG | P96R | XP_016881778.1 |