ENST00000524961.6:n.1931T>A
(SBF2)
|
|
|
ENST00000675281.2:c.5522T>A
(SBF2)
|
ENSP00000502491.1:p.Phe1841Tyr
|
|
ENST00000676324.2:c.*1755T>A
(SBF2)
|
ENSP00000502578.1:n.*1755T>A
|
|
ENST00000676387.2:c.5504T>A
(SBF2)
|
ENSP00000502779.1:p.Phe1835Tyr
|
|
ENST00000688344.1:c.5054T>A
(SBF2)
|
ENSP00000509987.1:p.Phe1685Tyr
|
|
ENST00000689128.1:c.5543T>A
(SBF2)
|
ENSP00000509587.1:p.Phe1848Tyr
|
|
ENST00000689258.1:c.5384T>A
(SBF2)
|
ENSP00000510475.1:p.Phe1795Tyr
|
|
ENST00000689342.1:c.1613T>A
(SBF2)
|
|
|
ENST00000689356.1:n.2618T>A
(SBF2)
|
|
|
ENST00000689940.1:c.5441T>A
(SBF2)
|
ENSP00000508452.1:p.Phe1814Tyr
|
|
ENST00000690437.1:n.1396T>A
(SBF2)
|
|
|
ENST00000690944.1:c.1527T>A
(SBF2)
|
|
|
ENST00000691616.1:n.1923T>A
(SBF2)
|
|
|
ENST00000692716.1:c.5318T>A
(SBF2)
|
ENSP00000509545.1:p.Phe1773Tyr
|
|
ENST00000693541.1:n.2366T>A
(SBF2)
|
|
|
ENST00000256190.13:c.5447T>A
(SBF2)
MANE Select
|
ENSP00000256190.8:p.Phe1816Tyr
|
|
ENST00000675281.1:c.5522T>A
(SBF2)
|
ENSP00000502491.1:p.Phe1841Tyr
|
|
ENST00000676324.1:c.*1755T>A
(SBF2)
|
ENSP00000502578.1:n.*1755T>A
|
|
ENST00000676387.1:c.5504T>A
(SBF2)
|
ENSP00000502779.1:p.Phe1835Tyr
|
|
ENST00000256190.12:c.5447T>A
(SBF2)
|
ENSP00000256190.8:p.Phe1816Tyr
|
|
ENST00000525040.5:n.750T>A
(SBF2)
|
|
|
ENST00000617179.4:c.5306T>A
(SBF2)
|
ENSP00000482806.1:p.Phe1769Tyr
|
|
NM_030962.3:c.5447T>A , LRG_267t1:c.5447T>A
(SBF2)
|
NP_112224.1:p.Phe1816Tyr
|
|
NR_036485.1:n.211+23008A>T
(SBF2-AS1)
|
|
|
XM_005253154.3:c.5543T>A
(SBF2)
|
XP_005253211.1:p.Phe1848Tyr
|
|
XM_005253155.3:c.5414T>A
(SBF2)
|
XP_005253212.1:p.Phe1805Tyr
|
|
XM_011520394.1:c.5429T>A
(SBF2)
|
XP_011518696.1:p.Phe1810Tyr
|
|
XR_931024.1:n.200+936A>T
|
|
|
XR_931025.1:n.200+936A>T
|
|
|
XM_005253154.5:c.5543T>A
(SBF2)
|
XP_005253211.1:p.Phe1848Tyr
|
|
XM_005253155.5:c.5414T>A
(SBF2)
|
XP_005253212.1:p.Phe1805Tyr
|
|
XM_011520394.3:c.5429T>A
(SBF2)
|
XP_011518696.1:p.Phe1810Tyr
|
|
XM_017018372.2:c.5405T>A
(SBF2)
|
XP_016873861.1:p.Phe1802Tyr
|
|
XM_017018373.2:c.5405T>A
(SBF2)
|
XP_016873862.1:p.Phe1802Tyr
|
|
XM_017018374.2:c.5318T>A
(SBF2)
|
XP_016873863.1:p.Phe1773Tyr
|
|
XM_017018375.2:c.5306T>A
(SBF2)
|
XP_016873864.1:p.Phe1769Tyr
|
|
XR_001747994.2:n.5554T>A
(SBF2)
|
|
|
XR_001748470.1:n.200+936A>T
|
|
|
XR_001748471.1:n.85+936A>T
|
|
|
NM_001386339.1:c.5543T>A
(SBF2)
|
NP_001373268.1:p.Phe1848Tyr
|
|
NM_001386342.1:c.5318T>A
(SBF2)
|
NP_001373271.1:p.Phe1773Tyr
|
|
NM_030962.4:c.5447T>A
(SBF2)
MANE Select
|
NP_112224.1:p.Phe1816Tyr
|
|