ENST00000682424.1:c.1051G>T
|
ENSP00000507321.1:p.Gly351Ter
|
|
ENST00000299427.12:c.1165G>T
MANE Select
|
ENSP00000299427.6:p.Gly389Ter
|
|
ENST00000436873.7:c.402G>T
|
|
|
ENST00000524924.2:n.285G>T
|
|
|
ENST00000533371.6:c.436G>T
|
ENSP00000437066.1:p.Gly146Ter
|
|
ENST00000642892.1:c.436G>T
|
ENSP00000494165.1:p.Gly146Ter
|
|
ENST00000643342.1:c.238G>T
|
|
|
ENST00000643439.1:c.*905G>T
|
ENSP00000495849.1:n.*905G>T
|
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ENST00000643479.1:n.1351G>T
|
|
|
ENST00000643516.1:c.674G>T
|
|
|
ENST00000644218.1:c.976G>T
|
ENSP00000493574.1:p.Gly326Ter
|
|
ENST00000644683.1:c.*618G>T
|
ENSP00000494085.1:n.*618G>T
|
|
ENST00000644810.1:c.886G>T
|
ENSP00000495895.1:p.Gly296Ter
|
|
ENST00000644831.1:n.1341G>T
|
|
|
ENST00000644933.1:c.*31G>T
|
ENSP00000496133.1:n.*31G>T
|
|
ENST00000645285.1:c.*31G>T
|
ENSP00000495058.1:n.*31G>T
|
|
ENST00000645331.1:n.2370G>T
|
|
|
ENST00000645620.1:c.436G>T
|
ENSP00000493657.1:p.Gly146Ter
|
|
ENST00000646691.1:n.940G>T
|
|
|
ENST00000646777.1:n.1498G>T
|
|
|
ENST00000647016.1:n.1645G>T
|
|
|
ENST00000647152.1:c.436G>T
|
ENSP00000495893.1:p.Gly146Ter
|
|
ENST00000647209.1:c.*1034G>T
|
ENSP00000495558.1:n.*1034G>T
|
|
ENST00000647346.1:n.2185G>T
|
|
|
ENST00000299427.10:c.1165G>T
|
ENSP00000299427.6:p.Gly389Ter
|
|
ENST00000524924.1:n.120G>T
|
|
|
ENST00000532191.1:n.218G>T
|
|
|
ENST00000533371.5:c.436G>T
|
ENSP00000437066.1:p.Gly146Ter
|
|
ENST00000611494.4:c.1165G>T
|
ENSP00000484546.1:p.Gly389Ter
|
|
NM_000391.3:c.1165G>T
|
NP_000382.3:p.Gly389Ter
|
|
NM_000391.4:c.1165G>T
MANE Select
|
NP_000382.3:p.Gly389Ter
|
|