Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001269053.1 | 359 | Missense Mutation | ATG,TTG | M92L | NP_001255982.1 |
NM_138812.3 | 359 | Missense Mutation | ATG,TTG | M92L | NP_620167.1 |
XM_005269549.4 | 359 | Missense Mutation | ATG,TTG | M92L | XP_005269606.1 |
XM_005269550.4 | 359 | Missense Mutation | ATG,TTG | M92L | XP_005269607.1 |
XM_011539334.2 | 359 | Missense Mutation | ATG,TTG | M92L | XP_011537636.1 |
XM_011539335.1 | 359 | Missense Mutation | ATG,TTG | M92L | XP_011537637.1 |
XM_017015749.1 | 359 | Missense Mutation | ATG,TTG | M92L | XP_016871238.1 |