ENST00000682424.1:c.323C>G
|
ENSP00000507321.1:p.Thr108Arg
|
|
ENST00000299427.12:c.437C>G
MANE Select
|
ENSP00000299427.6:p.Thr146Arg
|
|
ENST00000428886.7:n.525C>G
|
|
|
ENST00000436873.7:c.241C>G
|
|
|
ENST00000524788.2:n.1449C>G
|
|
|
ENST00000524903.2:n.1565C>G
|
|
|
ENST00000528571.6:c.*177C>G
|
ENSP00000434647.1:n.*177C>G
|
|
ENST00000528807.2:n.93C>G
|
|
|
ENST00000530040.2:n.466C>G
|
|
|
ENST00000533371.6:c.-293C>G
|
ENSP00000437066.1:n.-293C>G
|
|
ENST00000534644.6:n.438C>G
|
|
|
ENST00000642892.1:c.-240C>G
|
ENSP00000494165.1:n.-240C>G
|
|
ENST00000643439.1:c.*177C>G
|
ENSP00000495849.1:n.*177C>G
|
|
ENST00000643479.1:n.466C>G
|
|
|
ENST00000643516.1:c.324C>G
|
|
|
ENST00000644151.1:n.1729C>G
|
|
|
ENST00000644218.1:c.437C>G
|
ENSP00000493574.1:p.Thr146Arg
|
|
ENST00000644683.1:c.437C>G
|
ENSP00000494085.1:p.Thr146Arg
|
|
ENST00000644810.1:c.230-219C>G
|
ENSP00000495895.1:n.230-219C>G
|
|
ENST00000644831.1:n.466C>G
|
|
|
ENST00000644933.1:c.-293C>G
|
ENSP00000496133.1:n.-293C>G
|
|
ENST00000645020.1:n.1465C>G
|
|
|
ENST00000645285.1:c.-293C>G
|
ENSP00000495058.1:n.-293C>G
|
|
ENST00000645331.1:n.656C>G
|
|
|
ENST00000645620.1:c.-235C>G
|
ENSP00000493657.1:n.-235C>G
|
|
ENST00000646777.1:n.466C>G
|
|
|
ENST00000647016.1:n.770C>G
|
|
|
ENST00000647152.1:c.-293C>G
|
ENSP00000495893.1:n.-293C>G
|
|
ENST00000647209.1:c.*306C>G
|
ENSP00000495558.1:n.*306C>G
|
|
ENST00000647346.1:n.1457C>G
|
|
|
ENST00000299427.10:c.437C>G
|
ENSP00000299427.6:p.Thr146Arg
|
|
ENST00000428886.6:n.459C>G
|
|
|
ENST00000436873.6:c.437C>G
|
ENSP00000398136.2:p.Thr146Arg
|
|
ENST00000528571.5:c.*177C>G
|
ENSP00000434647.1:n.*177C>G
|
|
ENST00000530040.1:n.549C>G
|
|
|
ENST00000533371.5:c.-293C>G
|
ENSP00000437066.1:n.-293C>G
|
|
ENST00000534644.5:n.422C>G
|
|
|
ENST00000611494.4:c.437C>G
|
ENSP00000484546.1:p.Thr146Arg
|
|
NM_000391.3:c.437C>G
|
NP_000382.3:p.Thr146Arg
|
|
NM_000391.4:c.437C>G
MANE Select
|
NP_000382.3:p.Thr146Arg
|
|