Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005417.2 | 129 | UTR 5 | NP_001005417.1 | ||
NM_003780.4 | 129 | UTR 5 | NP_003771.1 | ||
NM_030587.2 | 129 | Missense Mutation | CCG,CTG | P18L | NP_085076.2 |
XM_017002716.1 | 129 | UTR 5 | XP_016858205.1 | ||
XM_017002717.1 | 129 | UTR 5 | XP_016858206.1 |