ENST00000698177.1:c.1308G>C
(SOX10)
|
ENSP00000513596.1:p.Gln436His
|
|
ENST00000690831.1:c.*714G>C
(SOX10)
|
ENSP00000510381.1:n.*714G>C
|
|
ENST00000396884.8:c.1092G>C
(SOX10)
MANE Select
|
ENSP00000380093.2:p.Gln364His
|
|
ENST00000651746.1:c.166-2800G>C
(SOX10)
|
|
|
ENST00000360880.6:c.1092G>C
(SOX10)
|
ENSP00000354130.2:p.Gln364His
|
|
ENST00000396884.6:c.1092G>C
(SOX10)
|
ENSP00000380093.2:p.Gln364His
|
|
ENST00000405557.5:c.293+6634C>G
(POLR2F)
|
ENSP00000384112.1:n.293+6634C>G
|
|
ENST00000407936.5:c.293+6634C>G
(POLR2F)
|
ENSP00000385725.1:n.293+6634C>G
|
|
ENST00000443002.5:c.*38+1494C>G
(POLR2F)
|
ENSP00000406826.1:n.*38+1494C>G
|
|
ENST00000446929.5:c.482+240G>C
(SOX10)
|
|
|
NM_001301130.1:c.293+6634C>G
(POLR2F)
|
NP_001288059.1:n.293+6634C>G
|
|
NM_001301131.1:c.293+6634C>G
(POLR2F)
|
NP_001288060.1:n.293+6634C>G
|
|
NM_006941.3:c.1092G>C , LRG_271t1:c.1092G>C
(SOX10)
|
NP_008872.1:p.Gln364His
|
|
XR_938243.1:n.158+1494C>G
|
|
|
NM_001363825.1:c.*38+1494C>G
(POLR2F)
|
NP_001350754.1:n.*38+1494C>G
|
|
NM_001301130.2:c.293+6634C>G
(POLR2F)
|
NP_001288059.1:n.293+6634C>G
|
|
NM_001301131.2:c.293+6634C>G
(POLR2F)
|
NP_001288060.1:n.293+6634C>G
|
|
NM_006941.4:c.1092G>C
(SOX10)
MANE Select
|
NP_008872.1:p.Gln364His
|
|