ENST00000394329.9:c.1632T>A
MANE Select
|
ENSP00000377862.4:p.Leu544=
|
|
ENST00000674496.2:c.-55+2066T>A
|
ENSP00000501473.2:n.-55+2066T>A
|
|
ENST00000394329.7:c.1632T>A
|
ENSP00000377862.3:p.Leu544=
|
|
NM_001291285.1:c.1632T>A
|
NP_001278214.1:p.Leu544=
|
|
NM_001291303.1:c.1632T>A
|
NP_001278232.1:p.Leu544=
|
|
NM_024582.4:c.1632T>A
|
NP_078858.4:p.Leu544=
|
|
XM_011532236.1:c.1632T>A
|
XP_011530538.1:p.Leu544=
|
|
XM_011532237.1:c.-55+2066T>A
|
XP_011530539.1:n.-55+2066T>A
|
|
XM_011532236.2:c.1632T>A
|
XP_011530538.1:p.Leu544=
|
|
XM_011532237.2:c.-55+2066T>A
|
XP_011530539.1:n.-55+2066T>A
|
|
NM_001291285.2:c.1632T>A
|
NP_001278214.1:p.Leu544=
|
|
NM_001291303.3:c.1632T>A
MANE Select
|
NP_001278232.1:p.Leu544=
|
|
NM_024582.5:c.1632T>A
|
NP_078858.4:p.Leu544=
|
|
NM_001291285.3:c.1632T>A
|
NP_001278214.1:p.Leu544=
|
|
NM_024582.6:c.1632T>A
|
NP_078858.4:p.Leu544=
|
|