ENST00000243964.7:c.3048G>A
MANE Select
|
ENSP00000243964.4:p.Glu1016=
|
|
ENST00000243964.6:c.3048G>A
|
ENSP00000243964.3:p.Glu1016=
|
|
ENST00000454036.6:c.3117G>A
|
ENSP00000387694.1:p.Glu1039=
|
|
ENST00000616201.4:c.1298-2154G>A
|
ENSP00000484585.1:n.1298-2154G>A
|
|
ENST00000616202.4:c.613-1979G>A
|
ENSP00000478369.1:n.613-1979G>A
|
|
ENST00000616933.4:c.*2366G>A
|
ENSP00000477569.1:n.*2366G>A
|
|
ENST00000626937.2:c.510-3097G>A
|
ENSP00000485953.1:n.510-3097G>A
|
|
ENST00000628413.1:n.564G>A
|
|
|
NM_001134771.1:c.3117G>A
|
NP_001128243.1:p.Glu1039=
|
|
NM_020708.4:c.3048G>A
|
NP_065759.1:p.Glu1016=
|
|
XM_017027981.1:c.3117G>A
|
XP_016883470.1:p.Glu1039=
|
|
NM_001134771.2:c.3117G>A
|
NP_001128243.1:p.Glu1039=
|
|
NM_020708.5:c.3048G>A
MANE Select
|
NP_065759.1:p.Glu1016=
|
|