ENST00000524961.6:n.1926T>A
(SBF2)
|
|
|
ENST00000675281.2:c.5517T>A
(SBF2)
|
ENSP00000502491.1:p.Ala1839=
|
|
ENST00000676324.2:c.*1750T>A
(SBF2)
|
ENSP00000502578.1:n.*1750T>A
|
|
ENST00000676387.2:c.5499T>A
(SBF2)
|
ENSP00000502779.1:p.Ala1833=
|
|
ENST00000688344.1:c.5049T>A
(SBF2)
|
ENSP00000509987.1:p.Ala1683=
|
|
ENST00000689128.1:c.5538T>A
(SBF2)
|
ENSP00000509587.1:p.Ala1846=
|
|
ENST00000689258.1:c.5379T>A
(SBF2)
|
ENSP00000510475.1:p.Ala1793=
|
|
ENST00000689342.1:c.1608T>A
(SBF2)
|
|
|
ENST00000689356.1:n.2613T>A
(SBF2)
|
|
|
ENST00000689940.1:c.5436T>A
(SBF2)
|
ENSP00000508452.1:p.Ala1812=
|
|
ENST00000690437.1:n.1391T>A
(SBF2)
|
|
|
ENST00000690944.1:c.1522T>A
(SBF2)
|
|
|
ENST00000691616.1:n.1918T>A
(SBF2)
|
|
|
ENST00000692716.1:c.5313T>A
(SBF2)
|
ENSP00000509545.1:p.Ala1771=
|
|
ENST00000693541.1:n.2361T>A
(SBF2)
|
|
|
ENST00000256190.13:c.5442T>A
(SBF2)
MANE Select
|
ENSP00000256190.8:p.Ala1814=
|
|
ENST00000675281.1:c.5517T>A
(SBF2)
|
ENSP00000502491.1:p.Ala1839=
|
|
ENST00000676324.1:c.*1750T>A
(SBF2)
|
ENSP00000502578.1:n.*1750T>A
|
|
ENST00000676387.1:c.5499T>A
(SBF2)
|
ENSP00000502779.1:p.Ala1833=
|
|
ENST00000256190.12:c.5442T>A
(SBF2)
|
ENSP00000256190.8:p.Ala1814=
|
|
ENST00000525040.5:n.745T>A
(SBF2)
|
|
|
ENST00000617179.4:c.5301T>A
(SBF2)
|
ENSP00000482806.1:p.Ala1767=
|
|
NM_030962.3:c.5442T>A , LRG_267t1:c.5442T>A
(SBF2)
|
NP_112224.1:p.Ala1814=
|
|
NR_036485.1:n.211+23013A>T
(SBF2-AS1)
|
|
|
XM_005253154.3:c.5538T>A
(SBF2)
|
XP_005253211.1:p.Ala1846=
|
|
XM_005253155.3:c.5409T>A
(SBF2)
|
XP_005253212.1:p.Ala1803=
|
|
XM_011520394.1:c.5424T>A
(SBF2)
|
XP_011518696.1:p.Ala1808=
|
|
XR_931024.1:n.200+941A>T
|
|
|
XR_931025.1:n.200+941A>T
|
|
|
XM_005253154.5:c.5538T>A
(SBF2)
|
XP_005253211.1:p.Ala1846=
|
|
XM_005253155.5:c.5409T>A
(SBF2)
|
XP_005253212.1:p.Ala1803=
|
|
XM_011520394.3:c.5424T>A
(SBF2)
|
XP_011518696.1:p.Ala1808=
|
|
XM_017018372.2:c.5400T>A
(SBF2)
|
XP_016873861.1:p.Ala1800=
|
|
XM_017018373.2:c.5400T>A
(SBF2)
|
XP_016873862.1:p.Ala1800=
|
|
XM_017018374.2:c.5313T>A
(SBF2)
|
XP_016873863.1:p.Ala1771=
|
|
XM_017018375.2:c.5301T>A
(SBF2)
|
XP_016873864.1:p.Ala1767=
|
|
XR_001747994.2:n.5549T>A
(SBF2)
|
|
|
XR_001748470.1:n.200+941A>T
|
|
|
XR_001748471.1:n.85+941A>T
|
|
|
NM_001386339.1:c.5538T>A
(SBF2)
|
NP_001373268.1:p.Ala1846=
|
|
NM_001386342.1:c.5313T>A
(SBF2)
|
NP_001373271.1:p.Ala1771=
|
|
NM_030962.4:c.5442T>A
(SBF2)
MANE Select
|
NP_112224.1:p.Ala1814=
|
|