|
ENST00000682424.1:c.173T>A
|
ENSP00000507321.1:p.Leu58His
|
|
|
ENST00000299427.12:c.287T>A
MANE Select
|
ENSP00000299427.6:p.Leu96His
|
|
|
ENST00000428886.7:n.375T>A
|
|
|
|
ENST00000436873.7:c.91T>A
|
|
|
|
ENST00000524788.2:n.1299T>A
|
|
|
|
ENST00000524903.2:n.1415T>A
|
|
|
|
ENST00000528571.6:c.*27T>A
|
ENSP00000434647.1:n.*27T>A
|
|
|
ENST00000530040.2:n.316T>A
|
|
|
|
ENST00000533371.6:c.-443T>A
|
ENSP00000437066.1:n.-443T>A
|
|
|
ENST00000534644.6:n.288T>A
|
|
|
|
ENST00000642892.1:c.-390T>A
|
ENSP00000494165.1:n.-390T>A
|
|
|
ENST00000643439.1:c.*27T>A
|
ENSP00000495849.1:n.*27T>A
|
|
|
ENST00000643479.1:n.316T>A
|
|
|
|
ENST00000643516.1:c.174T>A
|
|
|
|
ENST00000644151.1:n.1579T>A
|
|
|
|
ENST00000644218.1:c.287T>A
|
ENSP00000493574.1:p.Leu96His
|
|
|
ENST00000644683.1:c.287T>A
|
ENSP00000494085.1:p.Leu96His
|
|
|
ENST00000644810.1:c.230-566T>A
|
ENSP00000495895.1:n.230-566T>A
|
|
|
ENST00000644831.1:n.316T>A
|
|
|
|
ENST00000644933.1:c.-443T>A
|
ENSP00000496133.1:n.-443T>A
|
|
|
ENST00000645020.1:n.1315T>A
|
|
|
|
ENST00000645285.1:c.-443T>A
|
ENSP00000495058.1:n.-443T>A
|
|
|
ENST00000645331.1:n.309T>A
|
|
|
|
ENST00000645620.1:c.-385T>A
|
ENSP00000493657.1:n.-385T>A
|
|
|
ENST00000646777.1:n.316T>A
|
|
|
|
ENST00000647016.1:n.620T>A
|
|
|
|
ENST00000647152.1:c.-443T>A
|
ENSP00000495893.1:n.-443T>A
|
|
|
ENST00000647209.1:c.*156T>A
|
ENSP00000495558.1:n.*156T>A
|
|
|
ENST00000647346.1:n.1307T>A
|
|
|
|
ENST00000299427.10:c.287T>A
|
ENSP00000299427.6:p.Leu96His
|
|
|
ENST00000428886.6:n.309T>A
|
|
|
|
ENST00000436873.6:c.287T>A
|
ENSP00000398136.2:p.Leu96His
|
|
|
ENST00000528571.5:c.*27T>A
|
ENSP00000434647.1:n.*27T>A
|
|
|
ENST00000530040.1:n.399T>A
|
|
|
|
ENST00000533371.5:c.-443T>A
|
ENSP00000437066.1:n.-443T>A
|
|
|
ENST00000534644.5:n.272T>A
|
|
|
|
ENST00000611494.4:c.287T>A
|
ENSP00000484546.1:p.Leu96His
|
|
|
NM_000391.3:c.287T>A
|
NP_000382.3:p.Leu96His
|
|
|
NM_000391.4:c.287T>A
MANE Select
|
NP_000382.3:p.Leu96His
|
|
