ENST00000380649.8:c.1192G>C
MANE Select
|
ENSP00000370023.3:p.Asp398His
|
|
ENST00000492433.2:c.1192G>C
|
ENSP00000438039.2:p.Asp398His
|
|
ENST00000643057.1:c.*1083G>C
|
ENSP00000493761.1:n.*1083G>C
|
|
ENST00000643063.1:c.*238G>C
|
ENSP00000495353.1:n.*238G>C
|
|
ENST00000643233.1:c.*1083G>C
|
ENSP00000493880.1:n.*1083G>C
|
|
ENST00000644428.1:c.1192G>C
|
ENSP00000495560.1:p.Asp398His
|
|
ENST00000645274.1:c.1087G>C
|
ENSP00000493996.1:p.Asp363His
|
|
ENST00000646031.1:c.551G>C
|
|
|
ENST00000646483.1:c.1058G>C
|
ENSP00000496185.1:n.1058G>C
|
|
ENST00000380649.7:c.1192G>C
|
ENSP00000370023.3:p.Asp398His
|
|
NM_000182.4:c.1192G>C
|
NP_000173.2:p.Asp398His
|
|
NM_000182.5:c.1192G>C
MANE Select
|
NP_000173.2:p.Asp398His
|
|