ENST00000380649.8:c.1144G>C
MANE Select
|
ENSP00000370023.3:p.Asp382His
|
|
ENST00000492433.2:c.1144G>C
|
ENSP00000438039.2:p.Asp382His
|
|
ENST00000643057.1:c.*1035G>C
|
ENSP00000493761.1:n.*1035G>C
|
|
ENST00000643063.1:c.*190G>C
|
ENSP00000495353.1:n.*190G>C
|
|
ENST00000643233.1:c.*1035G>C
|
ENSP00000493880.1:n.*1035G>C
|
|
ENST00000644428.1:c.1144G>C
|
ENSP00000495560.1:p.Asp382His
|
|
ENST00000645274.1:c.1039G>C
|
ENSP00000493996.1:p.Asp347His
|
|
ENST00000646031.1:c.503G>C
|
|
|
ENST00000646483.1:c.1010G>C
|
ENSP00000496185.1:n.1010G>C
|
|
ENST00000380649.7:c.1144G>C
|
ENSP00000370023.3:p.Asp382His
|
|
NM_000182.4:c.1144G>C
|
NP_000173.2:p.Asp382His
|
|
NM_000182.5:c.1144G>C
MANE Select
|
NP_000173.2:p.Asp382His
|
|