ENST00000464710.2:n.2647G>C
|
|
|
ENST00000258743.10:c.471+870G>C
MANE Select
|
ENSP00000258743.5:n.471+870G>C
|
|
ENST00000258743.9:c.471+870G>C
|
ENSP00000258743.5:n.471+870G>C
|
|
ENST00000401630.7:c.402+870G>C
|
ENSP00000384928.3:n.402+870G>C
|
|
ENST00000404625.5:c.471+870G>C
|
ENSP00000385675.1:n.471+870G>C
|
|
ENST00000407492.5:c.243+870G>C
|
ENSP00000385043.1:n.243+870G>C
|
|
ENST00000485300.1:n.696+870G>C
|
|
|
NM_000600.3:c.471+870G>C
|
NP_000591.1:n.471+870G>C
|
|
XM_005249745.3:c.*744G>C
|
XP_005249802.1:n.*744G>C
|
|
XM_011515390.1:c.471+870G>C
|
XP_011513692.1:n.471+870G>C
|
|
XM_011515391.1:c.243+870G>C
|
XP_011513693.1:n.243+870G>C
|
|
NM_000600.4:c.471+870G>C
|
NP_000591.1:n.471+870G>C
|
|
NM_001318095.1:c.243+870G>C
|
NP_001305024.1:n.243+870G>C
|
|
XM_005249745.5:c.*744G>C
|
XP_005249802.1:n.*744G>C
|
|
XM_011515390.2:c.471+870G>C
|
XP_011513692.1:n.471+870G>C
|
|
NM_000600.5:c.471+870G>C
MANE Select
|
NP_000591.1:n.471+870G>C
|
|
NM_001318095.2:c.243+870G>C
|
NP_001305024.1:n.243+870G>C
|
|
NM_001371096.1:c.402+870G>C
|
NP_001358025.1:n.402+870G>C
|
|