ENST00000682424.1:c.165A>T
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ENSP00000507321.1:p.Pro55=
|
|
ENST00000299427.12:c.279A>T
MANE Select
|
ENSP00000299427.6:p.Pro93=
|
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ENST00000428886.7:n.367A>T
|
|
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ENST00000436873.7:c.83A>T
|
|
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ENST00000524788.2:n.1291A>T
|
|
|
ENST00000524903.2:n.1407A>T
|
|
|
ENST00000528571.6:c.*19A>T
|
ENSP00000434647.1:n.*19A>T
|
|
ENST00000530040.2:n.308A>T
|
|
|
ENST00000533371.6:c.-451A>T
|
ENSP00000437066.1:n.-451A>T
|
|
ENST00000534644.6:n.280A>T
|
|
|
ENST00000642892.1:c.-398A>T
|
ENSP00000494165.1:n.-398A>T
|
|
ENST00000643439.1:c.*19A>T
|
ENSP00000495849.1:n.*19A>T
|
|
ENST00000643479.1:n.308A>T
|
|
|
ENST00000643516.1:c.166A>T
|
|
|
ENST00000644151.1:n.1571A>T
|
|
|
ENST00000644218.1:c.279A>T
|
ENSP00000493574.1:p.Pro93=
|
|
ENST00000644683.1:c.279A>T
|
ENSP00000494085.1:p.Pro93=
|
|
ENST00000644810.1:c.230-574A>T
|
ENSP00000495895.1:n.230-574A>T
|
|
ENST00000644831.1:n.308A>T
|
|
|
ENST00000644933.1:c.-451A>T
|
ENSP00000496133.1:n.-451A>T
|
|
ENST00000645020.1:n.1307A>T
|
|
|
ENST00000645285.1:c.-451A>T
|
ENSP00000495058.1:n.-451A>T
|
|
ENST00000645331.1:n.301A>T
|
|
|
ENST00000645620.1:c.-393A>T
|
ENSP00000493657.1:n.-393A>T
|
|
ENST00000646777.1:n.308A>T
|
|
|
ENST00000647016.1:n.612A>T
|
|
|
ENST00000647152.1:c.-451A>T
|
ENSP00000495893.1:n.-451A>T
|
|
ENST00000647209.1:c.*148A>T
|
ENSP00000495558.1:n.*148A>T
|
|
ENST00000647346.1:n.1299A>T
|
|
|
ENST00000299427.10:c.279A>T
|
ENSP00000299427.6:p.Pro93=
|
|
ENST00000428886.6:n.301A>T
|
|
|
ENST00000436873.6:c.279A>T
|
ENSP00000398136.2:p.Pro93=
|
|
ENST00000528571.5:c.*19A>T
|
ENSP00000434647.1:n.*19A>T
|
|
ENST00000530040.1:n.391A>T
|
|
|
ENST00000533371.5:c.-451A>T
|
ENSP00000437066.1:n.-451A>T
|
|
ENST00000534644.5:n.264A>T
|
|
|
ENST00000611494.4:c.279A>T
|
ENSP00000484546.1:p.Pro93=
|
|
NM_000391.3:c.279A>T
|
NP_000382.3:p.Pro93=
|
|
NM_000391.4:c.279A>T
MANE Select
|
NP_000382.3:p.Pro93=
|
|