ENST00000682424.1:c.122A>C
|
ENSP00000507321.1:p.Tyr41Ser
|
|
ENST00000299427.12:c.236A>C
MANE Select
|
ENSP00000299427.6:p.Tyr79Ser
|
|
ENST00000428886.7:n.324A>C
|
|
|
ENST00000436873.7:c.40A>C
|
|
|
ENST00000524788.2:n.1248A>C
|
|
|
ENST00000524903.2:n.1364A>C
|
|
|
ENST00000528571.6:c.96A>C
|
ENSP00000434647.1:p.Ile32=
|
|
ENST00000530040.2:n.265A>C
|
|
|
ENST00000533371.6:c.-494A>C
|
ENSP00000437066.1:n.-494A>C
|
|
ENST00000534644.6:n.237A>C
|
|
|
ENST00000642892.1:c.-441A>C
|
ENSP00000494165.1:n.-441A>C
|
|
ENST00000643439.1:c.96A>C
|
ENSP00000495849.1:p.Ile32=
|
|
ENST00000643479.1:n.265A>C
|
|
|
ENST00000643516.1:c.123A>C
|
|
|
ENST00000644151.1:n.1528A>C
|
|
|
ENST00000644218.1:c.236A>C
|
ENSP00000493574.1:p.Tyr79Ser
|
|
ENST00000644683.1:c.236A>C
|
ENSP00000494085.1:p.Tyr79Ser
|
|
ENST00000644810.1:c.230-617A>C
|
ENSP00000495895.1:n.230-617A>C
|
|
ENST00000644831.1:n.265A>C
|
|
|
ENST00000644933.1:c.-494A>C
|
ENSP00000496133.1:n.-494A>C
|
|
ENST00000645020.1:n.1264A>C
|
|
|
ENST00000645285.1:c.-494A>C
|
ENSP00000495058.1:n.-494A>C
|
|
ENST00000645331.1:n.258A>C
|
|
|
ENST00000645620.1:c.-436A>C
|
ENSP00000493657.1:n.-436A>C
|
|
ENST00000646777.1:n.265A>C
|
|
|
ENST00000647016.1:n.569A>C
|
|
|
ENST00000647152.1:c.-494A>C
|
ENSP00000495893.1:n.-494A>C
|
|
ENST00000647209.1:c.*105A>C
|
ENSP00000495558.1:n.*105A>C
|
|
ENST00000647346.1:n.1256A>C
|
|
|
ENST00000299427.10:c.236A>C
|
ENSP00000299427.6:p.Tyr79Ser
|
|
ENST00000428886.6:n.258A>C
|
|
|
ENST00000436873.6:c.236A>C
|
ENSP00000398136.2:p.Tyr79Ser
|
|
ENST00000528571.5:c.96A>C
|
ENSP00000434647.1:p.Ile32=
|
|
ENST00000528917.1:n.537A>C
|
|
|
ENST00000530040.1:n.348A>C
|
|
|
ENST00000533371.5:c.-494A>C
|
ENSP00000437066.1:n.-494A>C
|
|
ENST00000534644.5:n.221A>C
|
|
|
ENST00000611494.4:c.236A>C
|
ENSP00000484546.1:p.Tyr79Ser
|
|
NM_000391.3:c.236A>C
|
NP_000382.3:p.Tyr79Ser
|
|
NM_000391.4:c.236A>C
MANE Select
|
NP_000382.3:p.Tyr79Ser
|
|