ENST00000682424.1:c.1052G>T
|
ENSP00000507321.1:p.Gly351Val
|
|
ENST00000299427.12:c.1166G>T
MANE Select
|
ENSP00000299427.6:p.Gly389Val
|
|
ENST00000436873.7:c.403G>T
|
|
|
ENST00000524924.2:n.286G>T
|
|
|
ENST00000533371.6:c.437G>T
|
ENSP00000437066.1:p.Gly146Val
|
|
ENST00000642892.1:c.437G>T
|
ENSP00000494165.1:p.Gly146Val
|
|
ENST00000643342.1:c.239G>T
|
|
|
ENST00000643439.1:c.*906G>T
|
ENSP00000495849.1:n.*906G>T
|
|
ENST00000643479.1:n.1352G>T
|
|
|
ENST00000643516.1:c.675G>T
|
|
|
ENST00000644218.1:c.977G>T
|
ENSP00000493574.1:p.Gly326Val
|
|
ENST00000644683.1:c.*619G>T
|
ENSP00000494085.1:n.*619G>T
|
|
ENST00000644810.1:c.887G>T
|
ENSP00000495895.1:p.Gly296Val
|
|
ENST00000644831.1:n.1342G>T
|
|
|
ENST00000644933.1:c.*32G>T
|
ENSP00000496133.1:n.*32G>T
|
|
ENST00000645285.1:c.*32G>T
|
ENSP00000495058.1:n.*32G>T
|
|
ENST00000645331.1:n.2371G>T
|
|
|
ENST00000645620.1:c.437G>T
|
ENSP00000493657.1:p.Gly146Val
|
|
ENST00000646691.1:n.941G>T
|
|
|
ENST00000646777.1:n.1499G>T
|
|
|
ENST00000647016.1:n.1646G>T
|
|
|
ENST00000647152.1:c.437G>T
|
ENSP00000495893.1:p.Gly146Val
|
|
ENST00000647209.1:c.*1035G>T
|
ENSP00000495558.1:n.*1035G>T
|
|
ENST00000647346.1:n.2186G>T
|
|
|
ENST00000299427.10:c.1166G>T
|
ENSP00000299427.6:p.Gly389Val
|
|
ENST00000524924.1:n.121G>T
|
|
|
ENST00000532191.1:n.219G>T
|
|
|
ENST00000533371.5:c.437G>T
|
ENSP00000437066.1:p.Gly146Val
|
|
ENST00000611494.4:c.1166G>T
|
ENSP00000484546.1:p.Gly389Val
|
|
NM_000391.3:c.1166G>T
|
NP_000382.3:p.Gly389Val
|
|
NM_000391.4:c.1166G>T
MANE Select
|
NP_000382.3:p.Gly389Val
|
|