|
NM_006767.4:c.263+1G>A
MANE Select
|
NP_006758.2:n.263+1G>A
|
|
ENST00000646124.2:c.263+1G>A
MANE Select
|
ENSP00000496779.1:n.263+1G>A
|
|
NM_006767.3:c.263+1G>A
|
NP_006758.2:n.263+1G>A
|
|
ENST00000215739.12:c.263+1G>A
|
ENSP00000215739.8:n.263+1G>A
|
|
ENST00000414985.5:c.263+1G>A
|
ENSP00000397247.1:n.263+1G>A
|
|
ENST00000443265.5:c.268+1G>A
|
ENSP00000406466.1:n.268+1G>A
|
|
ENST00000479606.5:n.409+1G>A
|
|
|
ENST00000493460.1:n.338+1G>A
|
|
|
ENST00000493460.2:n.338+1G>A
|
|
|
ENST00000642151.1:c.142G>A
|
|
|
ENST00000644435.1:c.169+1G>A
|
|
|
ENST00000645935.1:c.263+1G>A
|
ENSP00000493479.1:n.263+1G>A
|
|
ENST00000700578.1:c.263+1G>A
|
ENSP00000515073.1:n.263+1G>A
|