|
NM_006767.4:c.594-3C>T
MANE Select
|
NP_006758.2:n.594-3C>T
|
|
ENST00000646124.2:c.594-3C>T
MANE Select
|
ENSP00000496779.1:n.594-3C>T
|
|
NM_006767.3:c.594-3C>T
|
NP_006758.2:n.594-3C>T
|
|
ENST00000215739.12:c.594-3C>T
|
ENSP00000215739.8:n.594-3C>T
|
|
ENST00000414985.5:c.*160-3C>T
|
ENSP00000397247.1:n.*160-3C>T
|
|
ENST00000443265.5:c.*293-3C>T
|
ENSP00000406466.1:n.*293-3C>T
|
|
ENST00000479606.5:n.740-3C>T
|
|
|
ENST00000480895.1:n.290-3C>T
|
|
|
ENST00000642151.1:c.425-3C>T
|
|
|
ENST00000644435.1:c.416-3C>T
|
|
|
ENST00000646506.1:n.173-3C>T
|
|
|
ENST00000700578.1:c.594-3C>T
|
ENSP00000515073.1:n.594-3C>T
|