| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001253849.1 | 1173 | Intron | NP_001240778.1 | ||
| NM_001253850.1 | 1173 | Intron | NP_001240779.1 | ||
| NM_024626.3 | 1173 | Intron | NP_078902.2 | ||
| XM_011542143.2 | 1173 | Missense Mutation | CCG,CTG | P303L | XP_011540445.2 |
| XM_017002335.1 | 1173 | Missense Mutation | CCG,CTG | P258L | XP_016857824.1 |