ENST00000682424.1:c.254G>C
|
ENSP00000507321.1:p.Trp85Ser
|
|
ENST00000299427.12:c.368G>C
MANE Select
|
ENSP00000299427.6:p.Trp123Ser
|
|
ENST00000428886.7:n.456G>C
|
|
|
ENST00000436873.7:c.172G>C
|
|
|
ENST00000524788.2:n.1380G>C
|
|
|
ENST00000524903.2:n.1496G>C
|
|
|
ENST00000528571.6:c.*108G>C
|
ENSP00000434647.1:n.*108G>C
|
|
ENST00000530040.2:n.397G>C
|
|
|
ENST00000533371.6:c.-362G>C
|
ENSP00000437066.1:n.-362G>C
|
|
ENST00000534644.6:n.369G>C
|
|
|
ENST00000642892.1:c.-309G>C
|
ENSP00000494165.1:n.-309G>C
|
|
ENST00000643439.1:c.*108G>C
|
ENSP00000495849.1:n.*108G>C
|
|
ENST00000643479.1:n.397G>C
|
|
|
ENST00000643516.1:c.255G>C
|
|
|
ENST00000644151.1:n.1660G>C
|
|
|
ENST00000644218.1:c.368G>C
|
ENSP00000493574.1:p.Trp123Ser
|
|
ENST00000644683.1:c.368G>C
|
ENSP00000494085.1:p.Trp123Ser
|
|
ENST00000644810.1:c.230-485G>C
|
ENSP00000495895.1:n.230-485G>C
|
|
ENST00000644831.1:n.397G>C
|
|
|
ENST00000644933.1:c.-362G>C
|
ENSP00000496133.1:n.-362G>C
|
|
ENST00000645020.1:n.1396G>C
|
|
|
ENST00000645285.1:c.-362G>C
|
ENSP00000495058.1:n.-362G>C
|
|
ENST00000645331.1:n.390G>C
|
|
|
ENST00000645620.1:c.-304G>C
|
ENSP00000493657.1:n.-304G>C
|
|
ENST00000646777.1:n.397G>C
|
|
|
ENST00000647016.1:n.701G>C
|
|
|
ENST00000647152.1:c.-362G>C
|
ENSP00000495893.1:n.-362G>C
|
|
ENST00000647209.1:c.*237G>C
|
ENSP00000495558.1:n.*237G>C
|
|
ENST00000647346.1:n.1388G>C
|
|
|
ENST00000299427.10:c.368G>C
|
ENSP00000299427.6:p.Trp123Ser
|
|
ENST00000428886.6:n.390G>C
|
|
|
ENST00000436873.6:c.368G>C
|
ENSP00000398136.2:p.Trp123Ser
|
|
ENST00000528571.5:c.*108G>C
|
ENSP00000434647.1:n.*108G>C
|
|
ENST00000530040.1:n.480G>C
|
|
|
ENST00000533371.5:c.-362G>C
|
ENSP00000437066.1:n.-362G>C
|
|
ENST00000534644.5:n.353G>C
|
|
|
ENST00000611494.4:c.368G>C
|
ENSP00000484546.1:p.Trp123Ser
|
|
NM_000391.3:c.368G>C
|
NP_000382.3:p.Trp123Ser
|
|
NM_000391.4:c.368G>C
MANE Select
|
NP_000382.3:p.Trp123Ser
|
|