ENST00000682424.1:c.1115G>T
|
ENSP00000507321.1:p.Gly372Val
|
|
ENST00000299427.12:c.1229G>T
MANE Select
|
ENSP00000299427.6:p.Gly410Val
|
|
ENST00000436873.7:c.466G>T
|
|
|
ENST00000524924.2:n.349G>T
|
|
|
ENST00000533371.6:c.500G>T
|
ENSP00000437066.1:p.Gly167Val
|
|
ENST00000642892.1:c.500G>T
|
ENSP00000494165.1:p.Gly167Val
|
|
ENST00000643342.1:c.302G>T
|
|
|
ENST00000643439.1:c.*969G>T
|
ENSP00000495849.1:n.*969G>T
|
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ENST00000643479.1:n.1415G>T
|
|
|
ENST00000643516.1:c.738G>T
|
|
|
ENST00000644218.1:c.1040G>T
|
ENSP00000493574.1:p.Gly347Val
|
|
ENST00000644683.1:c.*682G>T
|
ENSP00000494085.1:n.*682G>T
|
|
ENST00000644810.1:c.950G>T
|
ENSP00000495895.1:p.Gly317Val
|
|
ENST00000644831.1:n.1405G>T
|
|
|
ENST00000644933.1:c.*95G>T
|
ENSP00000496133.1:n.*95G>T
|
|
ENST00000645285.1:c.*95G>T
|
ENSP00000495058.1:n.*95G>T
|
|
ENST00000645331.1:n.2434G>T
|
|
|
ENST00000645620.1:c.500G>T
|
ENSP00000493657.1:p.Gly167Val
|
|
ENST00000646691.1:n.1004G>T
|
|
|
ENST00000646777.1:n.1562G>T
|
|
|
ENST00000647016.1:n.1709G>T
|
|
|
ENST00000647152.1:c.500G>T
|
ENSP00000495893.1:p.Gly167Val
|
|
ENST00000647209.1:c.*1098G>T
|
ENSP00000495558.1:n.*1098G>T
|
|
ENST00000647346.1:n.2249G>T
|
|
|
ENST00000299427.10:c.1229G>T
|
ENSP00000299427.6:p.Gly410Val
|
|
ENST00000524924.1:n.184G>T
|
|
|
ENST00000532191.1:n.282G>T
|
|
|
ENST00000533371.5:c.500G>T
|
ENSP00000437066.1:p.Gly167Val
|
|
ENST00000611494.4:c.1229G>T
|
ENSP00000484546.1:p.Gly410Val
|
|
NM_000391.3:c.1229G>T
|
NP_000382.3:p.Gly410Val
|
|
NM_000391.4:c.1229G>T
MANE Select
|
NP_000382.3:p.Gly410Val
|
|