| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001251845.1 | 137 | Missense Mutation | ATG,TTG | M1L | NP_001238774.1 |
| NM_003304.4 | 137 | Missense Mutation | ATG,TTG | M1L | NP_003295.1 |
| XM_005247738.3 | 137 | Intron | XP_005247795.1 | ||
| XM_005247739.2 | 137 | UTR 5 | XP_005247796.1 | ||
| XM_017007121.1 | 137 | Intron | XP_016862610.1 | ||
| XM_017007122.1 | 137 | Intron | XP_016862611.1 |