ENST00000682338.1:c.498+134G>T
|
ENSP00000507062.1:n.498+134G>T
|
|
ENST00000682793.1:c.498+134G>T
|
ENSP00000506910.1:n.498+134G>T
|
|
ENST00000682838.1:c.*157-165G>T
|
ENSP00000507652.1:n.*157-165G>T
|
|
ENST00000683578.1:c.498+134G>T
|
ENSP00000507430.1:n.498+134G>T
|
|
ENST00000683661.1:n.2033+134G>T
|
|
|
ENST00000684324.1:c.498+134G>T
|
ENSP00000507937.1:n.498+134G>T
|
|
ENST00000684545.1:c.498+134G>T
|
ENSP00000506733.1:n.498+134G>T
|
|
ENST00000684714.1:c.498+134G>T
|
ENSP00000506861.1:n.498+134G>T
|
|
ENST00000375679.9:c.498+134G>T
MANE Select
|
ENSP00000364831.5:n.498+134G>T
|
|
ENST00000375679.8:c.498+134G>T
|
ENSP00000364831.4:n.498+134G>T
|
|
ENST00000619181.4:c.498+134G>T
|
ENSP00000483866.1:n.498+134G>T
|
|
NM_000085.4:c.498+134G>T
|
NP_000076.2:n.498+134G>T
|
|
XM_011540619.1:c.339+134G>T
|
XP_011538921.1:n.339+134G>T
|
|
XM_011540620.1:c.498+134G>T
|
XP_011538922.1:n.498+134G>T
|
|
NM_000085.5:c.498+134G>T
MANE Select
|
NP_000076.2:n.498+134G>T
|
|