ENST00000682424.1:c.1068G>C
|
ENSP00000507321.1:p.Gln356His
|
|
ENST00000299427.12:c.1182G>C
MANE Select
|
ENSP00000299427.6:p.Gln394His
|
|
ENST00000436873.7:c.419G>C
|
|
|
ENST00000524924.2:n.302G>C
|
|
|
ENST00000533371.6:c.453G>C
|
ENSP00000437066.1:p.Gln151His
|
|
ENST00000642892.1:c.453G>C
|
ENSP00000494165.1:p.Gln151His
|
|
ENST00000643342.1:c.255G>C
|
|
|
ENST00000643439.1:c.*922G>C
|
ENSP00000495849.1:n.*922G>C
|
|
ENST00000643479.1:n.1368G>C
|
|
|
ENST00000643516.1:c.691G>C
|
|
|
ENST00000644218.1:c.993G>C
|
ENSP00000493574.1:p.Gln331His
|
|
ENST00000644683.1:c.*635G>C
|
ENSP00000494085.1:n.*635G>C
|
|
ENST00000644810.1:c.903G>C
|
ENSP00000495895.1:p.Gln301His
|
|
ENST00000644831.1:n.1358G>C
|
|
|
ENST00000644933.1:c.*48G>C
|
ENSP00000496133.1:n.*48G>C
|
|
ENST00000645285.1:c.*48G>C
|
ENSP00000495058.1:n.*48G>C
|
|
ENST00000645331.1:n.2387G>C
|
|
|
ENST00000645620.1:c.453G>C
|
ENSP00000493657.1:p.Gln151His
|
|
ENST00000646691.1:n.957G>C
|
|
|
ENST00000646777.1:n.1515G>C
|
|
|
ENST00000647016.1:n.1662G>C
|
|
|
ENST00000647152.1:c.453G>C
|
ENSP00000495893.1:p.Gln151His
|
|
ENST00000647209.1:c.*1051G>C
|
ENSP00000495558.1:n.*1051G>C
|
|
ENST00000647346.1:n.2202G>C
|
|
|
ENST00000299427.10:c.1182G>C
|
ENSP00000299427.6:p.Gln394His
|
|
ENST00000524924.1:n.137G>C
|
|
|
ENST00000532191.1:n.235G>C
|
|
|
ENST00000533371.5:c.453G>C
|
ENSP00000437066.1:p.Gln151His
|
|
ENST00000611494.4:c.1182G>C
|
ENSP00000484546.1:p.Gln394His
|
|
NM_000391.3:c.1182G>C
|
NP_000382.3:p.Gln394His
|
|
NM_000391.4:c.1182G>C
MANE Select
|
NP_000382.3:p.Gln394His
|
|