ENST00000573854.6:c.1281+584C>T
MANE Select
|
ENSP00000459451.1:n.1281+584C>T
|
|
ENST00000219054.10:c.1281+584C>T
|
ENSP00000219054.6:n.1281+584C>T
|
|
ENST00000396104.2:c.1281+584C>T
|
ENSP00000379411.2:n.1281+584C>T
|
|
ENST00000417235.6:c.1044+584C>T
|
ENSP00000392169.2:n.1044+584C>T
|
|
ENST00000570698.5:n.1456+584C>T
|
|
|
ENST00000572843.5:n.1476+584C>T
|
|
|
ENST00000573854.5:c.1281+584C>T
|
ENSP00000459451.1:n.1281+584C>T
|
|
ENST00000575558.5:n.1210+584C>T
|
|
|
ENST00000575690.5:c.1281+584C>T
|
ENSP00000460349.1:n.1281+584C>T
|
|
ENST00000576101.1:n.1033+584C>T
|
|
|
NM_001010845.2:c.1281+584C>T
|
NP_001010845.1:n.1281+584C>T
|
|
NM_001308169.1:c.1044+584C>T
|
NP_001295098.1:n.1044+584C>T
|
|
NM_001308172.1:c.1281+584C>T
|
NP_001295101.1:n.1281+584C>T
|
|
NM_001308954.1:c.1281+584C>T
|
NP_001295883.1:n.1281+584C>T
|
|
XR_243259.2:n.2281+584C>T
|
|
|
XM_017022923.1:c.1281+584C>T
|
XP_016878412.1:n.1281+584C>T
|
|
XM_017022924.2:c.*187C>T
|
XP_016878413.1:n.*187C>T
|
|
XM_017022925.1:c.1044+584C>T
|
XP_016878414.1:n.1044+584C>T
|
|
XM_017022926.2:c.594+584C>T
|
XP_016878415.1:n.594+584C>T
|
|
XR_001751834.2:n.2490+584C>T
|
|
|
NM_001308172.2:c.1281+584C>T
MANE Select
|
NP_001295101.1:n.1281+584C>T
|
|
NM_001308169.2:c.1044+584C>T
|
NP_001295098.1:n.1044+584C>T
|
|
NM_001308954.2:c.1281+584C>T
|
NP_001295883.1:n.1281+584C>T
|
|