|
ENST00000704289.1:c.*976T>G
|
ENSP00000515816.1:n.*976T>G
|
|
|
ENST00000315285.9:c.1316T>G
MANE Select
|
ENSP00000320885.3:p.Phe439Cys
|
|
|
ENST00000621856.2:c.1313T>G
|
ENSP00000482496.2:p.Phe438Cys
|
|
|
ENST00000642281.1:c.1053T>G
|
|
|
|
ENST00000642455.1:c.1217T>G
|
ENSP00000493827.1:p.Phe406Cys
|
|
|
ENST00000642751.1:c.1090T>G
|
|
|
|
ENST00000642999.1:c.1058T>G
|
ENSP00000496589.1:p.Phe353Cys
|
|
|
ENST00000643327.1:c.475T>G
|
|
|
|
ENST00000643334.1:c.896T>G
|
|
|
|
ENST00000644408.1:c.1192T>G
|
|
|
|
ENST00000644954.1:c.962T>G
|
ENSP00000494312.1:p.Phe321Cys
|
|
|
ENST00000645159.1:n.2053T>G
|
|
|
|
ENST00000645671.1:c.766T>G
|
|
|
|
ENST00000645730.1:c.593-476T>G
|
|
|
|
ENST00000646082.1:c.962T>G
|
|
|
|
ENST00000646571.1:c.1220T>G
|
ENSP00000495015.1:p.Phe407Cys
|
|
|
ENST00000647007.1:n.1008T>G
|
|
|
|
ENST00000647133.1:c.816T>G
|
|
|
|
ENST00000315285.7:c.1316T>G
|
ENSP00000320885.3:p.Phe439Cys
|
|
|
ENST00000345662.5:c.1220T>G
|
ENSP00000340817.1:p.Phe407Cys
|
|
|
ENST00000615843.4:c.1316T>G
|
ENSP00000480893.1:p.Phe439Cys
|
|
|
ENST00000621856.1:c.1058T>G
|
ENSP00000482496.1:p.Phe353Cys
|
|
|
NM_014946.3:c.1316T>G , LRG_714t1:c.1316T>G
|
NP_055761.2:p.Phe439Cys
|
|
|
NM_199436.1:c.1220T>G
|
NP_955468.1:p.Phe407Cys
|
|
|
XM_005264516.3:c.1313T>G
|
XP_005264573.1:p.Phe438Cys
|
|
|
XM_011533067.1:c.1316T>G
|
XP_011531369.1:p.Phe439Cys
|
|
|
NM_001363823.1:c.1313T>G
|
NP_001350752.1:p.Phe438Cys
|
|
|
NM_001363875.1:c.1217T>G
|
NP_001350804.1:p.Phe406Cys
|
|
|
XM_005264516.5:c.1313T>G
|
XP_005264573.1:p.Phe438Cys
|
|
|
XM_011533067.2:c.1316T>G
|
XP_011531369.1:p.Phe439Cys
|
|
|
XM_017004778.2:c.1220T>G
|
XP_016860267.1:p.Phe407Cys
|
|
|
NM_001363823.2:c.1313T>G
|
NP_001350752.1:p.Phe438Cys
|
|
|
NM_001363875.2:c.1217T>G
|
NP_001350804.1:p.Phe406Cys
|
|
|
NM_001377959.1:c.1220T>G
|
NP_001364888.1:p.Phe407Cys
|
|
|
NM_014946.4:c.1316T>G
MANE Select
|
NP_055761.2:p.Phe439Cys
|
|
|
NM_199436.2:c.1220T>G
|
NP_955468.1:p.Phe407Cys
|
|
