ENST00000682424.1:c.1259G>T
|
ENSP00000507321.1:p.Gly420Val
|
|
ENST00000299427.12:c.1373G>T
MANE Select
|
ENSP00000299427.6:p.Gly458Val
|
|
ENST00000524611.2:n.233G>T
|
|
|
ENST00000524924.2:n.493G>T
|
|
|
ENST00000533371.6:c.644G>T
|
ENSP00000437066.1:p.Gly215Val
|
|
ENST00000642892.1:c.644G>T
|
ENSP00000494165.1:p.Gly215Val
|
|
ENST00000643342.1:c.446G>T
|
|
|
ENST00000643439.1:c.*1113G>T
|
ENSP00000495849.1:n.*1113G>T
|
|
ENST00000643479.1:n.1559G>T
|
|
|
ENST00000643516.1:c.882G>T
|
|
|
ENST00000644218.1:c.1184G>T
|
ENSP00000493574.1:p.Gly395Val
|
|
ENST00000644683.1:c.*826G>T
|
ENSP00000494085.1:n.*826G>T
|
|
ENST00000644810.1:c.1094G>T
|
ENSP00000495895.1:p.Gly365Val
|
|
ENST00000644831.1:n.1549G>T
|
|
|
ENST00000644933.1:c.*239G>T
|
ENSP00000496133.1:n.*239G>T
|
|
ENST00000645285.1:c.*239G>T
|
ENSP00000495058.1:n.*239G>T
|
|
ENST00000645331.1:n.2578G>T
|
|
|
ENST00000645620.1:c.644G>T
|
ENSP00000493657.1:p.Gly215Val
|
|
ENST00000646691.1:n.1260G>T
|
|
|
ENST00000646777.1:n.1706G>T
|
|
|
ENST00000647016.1:n.1853G>T
|
|
|
ENST00000647152.1:c.644G>T
|
ENSP00000495893.1:p.Gly215Val
|
|
ENST00000647209.1:c.*1242G>T
|
ENSP00000495558.1:n.*1242G>T
|
|
ENST00000647346.1:n.2393G>T
|
|
|
ENST00000299427.10:c.1373G>T
|
ENSP00000299427.6:p.Gly458Val
|
|
ENST00000524611.1:n.251G>T
|
|
|
ENST00000532191.1:n.426G>T
|
|
|
ENST00000533371.5:c.644G>T
|
ENSP00000437066.1:p.Gly215Val
|
|
ENST00000611494.4:c.1373G>T
|
ENSP00000484546.1:p.Gly458Val
|
|
NM_000391.3:c.1373G>T
|
NP_000382.3:p.Gly458Val
|
|
NM_000391.4:c.1373G>T
MANE Select
|
NP_000382.3:p.Gly458Val
|
|