|
NM_006767.4:c.510-2A>G
MANE Select
|
NP_006758.2:n.510-2A>G
|
|
ENST00000646124.2:c.510-2A>G
MANE Select
|
ENSP00000496779.1:n.510-2A>G
|
|
NM_006767.3:c.510-2A>G
|
NP_006758.2:n.510-2A>G
|
|
ENST00000215739.12:c.510-2A>G
|
ENSP00000215739.8:n.510-2A>G
|
|
ENST00000414985.5:c.*76-2A>G
|
ENSP00000397247.1:n.*76-2A>G
|
|
ENST00000443265.5:c.*209-2A>G
|
ENSP00000406466.1:n.*209-2A>G
|
|
ENST00000479606.5:n.656-2A>G
|
|
|
ENST00000480895.1:n.206-2A>G
|
|
|
ENST00000642151.1:c.341-2A>G
|
|
|
ENST00000644435.1:c.415+669A>G
|
|
|
ENST00000646506.1:n.89-2A>G
|
|
|
ENST00000700578.1:c.510-2A>G
|
ENSP00000515073.1:n.510-2A>G
|