Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_139170.2 | 138 | Missense Mutation | ATG,GTG | M20V | NP_631909.2 |
XM_005255144.3 | 138 | Intron | XP_005255201.1 | ||
XM_017022975.1 | 138 | Missense Mutation | ATG,GTG | M43V | XP_016878464.1 |
XM_017022976.1 | 138 | Missense Mutation | ATG,GTG | M20V | XP_016878465.1 |