ENST00000682424.1:c.1118G>T
|
ENSP00000507321.1:p.Gly373Val
|
|
ENST00000299427.12:c.1232G>T
MANE Select
|
ENSP00000299427.6:p.Gly411Val
|
|
ENST00000436873.7:c.469G>T
|
|
|
ENST00000524924.2:n.352G>T
|
|
|
ENST00000533371.6:c.503G>T
|
ENSP00000437066.1:p.Gly168Val
|
|
ENST00000642892.1:c.503G>T
|
ENSP00000494165.1:p.Gly168Val
|
|
ENST00000643342.1:c.305G>T
|
|
|
ENST00000643439.1:c.*972G>T
|
ENSP00000495849.1:n.*972G>T
|
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ENST00000643479.1:n.1418G>T
|
|
|
ENST00000643516.1:c.741G>T
|
|
|
ENST00000644218.1:c.1043G>T
|
ENSP00000493574.1:p.Gly348Val
|
|
ENST00000644683.1:c.*685G>T
|
ENSP00000494085.1:n.*685G>T
|
|
ENST00000644810.1:c.953G>T
|
ENSP00000495895.1:p.Gly318Val
|
|
ENST00000644831.1:n.1408G>T
|
|
|
ENST00000644933.1:c.*98G>T
|
ENSP00000496133.1:n.*98G>T
|
|
ENST00000645285.1:c.*98G>T
|
ENSP00000495058.1:n.*98G>T
|
|
ENST00000645331.1:n.2437G>T
|
|
|
ENST00000645620.1:c.503G>T
|
ENSP00000493657.1:p.Gly168Val
|
|
ENST00000646691.1:n.1007G>T
|
|
|
ENST00000646777.1:n.1565G>T
|
|
|
ENST00000647016.1:n.1712G>T
|
|
|
ENST00000647152.1:c.503G>T
|
ENSP00000495893.1:p.Gly168Val
|
|
ENST00000647209.1:c.*1101G>T
|
ENSP00000495558.1:n.*1101G>T
|
|
ENST00000647346.1:n.2252G>T
|
|
|
ENST00000299427.10:c.1232G>T
|
ENSP00000299427.6:p.Gly411Val
|
|
ENST00000524924.1:n.187G>T
|
|
|
ENST00000532191.1:n.285G>T
|
|
|
ENST00000533371.5:c.503G>T
|
ENSP00000437066.1:p.Gly168Val
|
|
ENST00000611494.4:c.1232G>T
|
ENSP00000484546.1:p.Gly411Val
|
|
NM_000391.3:c.1232G>T
|
NP_000382.3:p.Gly411Val
|
|
NM_000391.4:c.1232G>T
MANE Select
|
NP_000382.3:p.Gly411Val
|
|