| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184720.1 | 347 | Silent Mutation | CTC,CTT | L38L | NP_001171649.1 |
| NM_001184721.1 | 347 | Silent Mutation | CTC,CTT | L38L | NP_001171650.1 |
| NM_004130.3 | 347 | Silent Mutation | CTC,CTT | L38L | NP_004121.2 |
| XM_017006275.1 | 347 | Intron | XP_016861764.1 | ||
| XM_017006276.1 | 347 | Intron | XP_016861765.1 |