|
ENST00000402738.6:c.386+26G>T
MANE Select
|
ENSP00000385684.1:n.386+26G>T
|
|
|
ENST00000512194.2:c.386+26G>T
|
ENSP00000421021.2:n.386+26G>T
|
|
|
ENST00000264345.7:c.386+26G>T
|
ENSP00000264345.3:n.386+26G>T
|
|
|
ENST00000402738.5:c.386+26G>T
|
ENSP00000385684.1:n.386+26G>T
|
|
|
ENST00000407637.5:c.386+26G>T
|
ENSP00000384005.1:n.386+26G>T
|
|
|
ENST00000431413.5:c.386+26G>T
|
ENSP00000405863.1:n.386+26G>T
|
|
|
ENST00000452979.5:c.386+26G>T
|
ENSP00000406210.1:n.386+26G>T
|
|
|
NM_001271602.1:c.32+26G>T
|
NP_001258531.1:n.32+26G>T
|
|
|
NM_014606.2:c.386+26G>T
|
NP_055421.1:n.386+26G>T
|
|
|
XM_005263327.2:c.386+26G>T
|
XP_005263384.1:n.386+26G>T
|
|
|
XM_005263329.2:c.386+26G>T
|
XP_005263386.1:n.386+26G>T
|
|
|
XM_005263330.2:c.386+26G>T
|
XP_005263387.1:n.386+26G>T
|
|
|
XM_005263331.1:c.386+26G>T
|
XP_005263388.1:n.386+26G>T
|
|
|
XM_005263332.2:c.386+26G>T
|
XP_005263389.1:n.386+26G>T
|
|
|
NM_001318505.1:c.386+26G>T
|
NP_001305434.1:n.386+26G>T
|
|
|
XM_005263327.3:c.386+26G>T
|
XP_005263384.1:n.386+26G>T
|
|
|
XM_005263329.4:c.386+26G>T
|
XP_005263386.1:n.386+26G>T
|
|
|
XM_005263330.4:c.386+26G>T
|
XP_005263387.1:n.386+26G>T
|
|
|
XM_005263331.2:c.386+26G>T
|
XP_005263388.1:n.386+26G>T
|
|
|
XM_005263332.4:c.386+26G>T
|
XP_005263389.1:n.386+26G>T
|
|
|
XM_017008806.2:c.386+26G>T
|
XP_016864295.1:n.386+26G>T
|
|
|
XM_017008807.1:c.32+26G>T
|
XP_016864296.1:n.32+26G>T
|
|
|
NM_014606.3:c.386+26G>T
MANE Select
|
NP_055421.1:n.386+26G>T
|
|
|
NM_001271602.2:c.32+26G>T
|
NP_001258531.1:n.32+26G>T
|
|
|
NM_001318505.2:c.386+26G>T
|
NP_001305434.1:n.386+26G>T
|
|
|
NM_001375477.1:c.32+26G>T
|
NP_001362406.1:n.32+26G>T
|
|
|
NM_001375478.1:c.386+26G>T
|
NP_001362407.1:n.386+26G>T
|
|
|
NM_001375479.1:c.386+26G>T
|
NP_001362408.1:n.386+26G>T
|
|
|
NM_001375480.1:c.386+26G>T
|
NP_001362409.1:n.386+26G>T
|
|
|
NM_001375481.1:c.32+26G>T
|
NP_001362410.1:n.32+26G>T
|
|
|
NM_001375482.1:c.386+26G>T
|
NP_001362411.1:n.386+26G>T
|
|
|
NM_001375483.1:c.386+26G>T
|
NP_001362412.1:n.386+26G>T
|
|
