ENST00000698177.1:c.594C>A
(SOX10)
|
ENSP00000513596.1:p.Tyr198Ter
|
|
ENST00000690831.1:c.378C>A
(SOX10)
|
ENSP00000510381.1:p.Tyr126Ter
|
|
ENST00000396884.8:c.378C>A
(SOX10)
MANE Select
|
ENSP00000380093.2:p.Tyr126Ter
|
|
ENST00000652356.1:n.667C>A
(SOX10)
|
|
|
ENST00000360880.6:c.378C>A
(SOX10)
|
ENSP00000354130.2:p.Tyr126Ter
|
|
ENST00000396884.6:c.378C>A
(SOX10)
|
ENSP00000380093.2:p.Tyr126Ter
|
|
ENST00000405557.5:c.293+16237G>T
(POLR2F)
|
ENSP00000384112.1:n.293+16237G>T
|
|
ENST00000407936.5:c.294-2747G>T
(POLR2F)
|
ENSP00000385725.1:n.294-2747G>T
|
|
ENST00000427770.1:c.378C>A
(SOX10)
|
ENSP00000414853.1:p.Tyr126Ter
|
|
ENST00000443002.5:c.*39-1645G>T
(POLR2F)
|
ENSP00000406826.1:n.*39-1645G>T
|
|
ENST00000446929.5:c.8C>A
(SOX10)
|
|
|
ENST00000470555.1:n.70+932C>A
(SOX10)
|
|
|
NM_001301130.1:c.294-2747G>T
(POLR2F)
|
NP_001288059.1:n.294-2747G>T
|
|
NM_001301131.1:c.293+16237G>T
(POLR2F)
|
NP_001288060.1:n.293+16237G>T
|
|
NM_006941.3:c.378C>A , LRG_271t1:c.378C>A
(SOX10)
|
NP_008872.1:p.Tyr126Ter
|
|
XR_938243.1:n.158+11097G>T
|
|
|
NM_001363825.1:c.*38+11097G>T
(POLR2F)
|
NP_001350754.1:n.*38+11097G>T
|
|
NM_001301130.2:c.294-2747G>T
(POLR2F)
|
NP_001288059.1:n.294-2747G>T
|
|
NM_001301131.2:c.293+16237G>T
(POLR2F)
|
NP_001288060.1:n.293+16237G>T
|
|
NM_006941.4:c.378C>A
(SOX10)
MANE Select
|
NP_008872.1:p.Tyr126Ter
|
|