| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000995.4 | 194 | Missense Mutation | ATG,GTG | M48V | NP_000986.2 |
| NM_001319232.1 | 194 | Intron | NP_001306161.1 | ||
| NM_001319234.1 | 194 | Missense Mutation | ATG,GTG | M48V | NP_001306163.1 |
| NM_001319235.1 | 194 | Intron | NP_001306164.1 | ||
| NM_001319236.1 | 194 | Intron | NP_001306165.1 | ||
| NM_033625.3 | 194 | Missense Mutation | ATG,GTG | M48V | NP_296374.1 |