Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042469.1 | 449 | Intron | NP_001035934.2 | ||
NM_001042470.1 | 449 | Intron | NP_001035935.2 | ||
NM_001130069.2 | 449 | Missense Mutation | ATG,GTG | M140V | NP_001123541.1 |
NM_001146333.1 | 449 | Missense Mutation | ATG,GTG | M33V | NP_001139805.1 |
NM_015411.2 | 449 | Missense Mutation | ATG,GTG | M140V | NP_056226.2 |
XM_011515254.2 | 449 | Missense Mutation | ATG,GTG | M140V | XP_011513556.1 |
XM_017011939.1 | 449 | Missense Mutation | ATG,GTG | M140V | XP_016867428.1 |
XM_017011940.1 | 449 | Intron | XP_016867429.1 |