ENST00000524961.6:n.1930T>G
(SBF2)
|
|
|
ENST00000675281.2:c.5521T>G
(SBF2)
|
ENSP00000502491.1:p.Phe1841Val
|
|
ENST00000676324.2:c.*1754T>G
(SBF2)
|
ENSP00000502578.1:n.*1754T>G
|
|
ENST00000676387.2:c.5503T>G
(SBF2)
|
ENSP00000502779.1:p.Phe1835Val
|
|
ENST00000688344.1:c.5053T>G
(SBF2)
|
ENSP00000509987.1:p.Phe1685Val
|
|
ENST00000689128.1:c.5542T>G
(SBF2)
|
ENSP00000509587.1:p.Phe1848Val
|
|
ENST00000689258.1:c.5383T>G
(SBF2)
|
ENSP00000510475.1:p.Phe1795Val
|
|
ENST00000689342.1:c.1612T>G
(SBF2)
|
|
|
ENST00000689356.1:n.2617T>G
(SBF2)
|
|
|
ENST00000689940.1:c.5440T>G
(SBF2)
|
ENSP00000508452.1:p.Phe1814Val
|
|
ENST00000690437.1:n.1395T>G
(SBF2)
|
|
|
ENST00000690944.1:c.1526T>G
(SBF2)
|
|
|
ENST00000691616.1:n.1922T>G
(SBF2)
|
|
|
ENST00000692716.1:c.5317T>G
(SBF2)
|
ENSP00000509545.1:p.Phe1773Val
|
|
ENST00000693541.1:n.2365T>G
(SBF2)
|
|
|
ENST00000256190.13:c.5446T>G
(SBF2)
MANE Select
|
ENSP00000256190.8:p.Phe1816Val
|
|
ENST00000675281.1:c.5521T>G
(SBF2)
|
ENSP00000502491.1:p.Phe1841Val
|
|
ENST00000676324.1:c.*1754T>G
(SBF2)
|
ENSP00000502578.1:n.*1754T>G
|
|
ENST00000676387.1:c.5503T>G
(SBF2)
|
ENSP00000502779.1:p.Phe1835Val
|
|
ENST00000256190.12:c.5446T>G
(SBF2)
|
ENSP00000256190.8:p.Phe1816Val
|
|
ENST00000525040.5:n.749T>G
(SBF2)
|
|
|
ENST00000617179.4:c.5305T>G
(SBF2)
|
ENSP00000482806.1:p.Phe1769Val
|
|
NM_030962.3:c.5446T>G , LRG_267t1:c.5446T>G
(SBF2)
|
NP_112224.1:p.Phe1816Val
|
|
NR_036485.1:n.211+23009A>C
(SBF2-AS1)
|
|
|
XM_005253154.3:c.5542T>G
(SBF2)
|
XP_005253211.1:p.Phe1848Val
|
|
XM_005253155.3:c.5413T>G
(SBF2)
|
XP_005253212.1:p.Phe1805Val
|
|
XM_011520394.1:c.5428T>G
(SBF2)
|
XP_011518696.1:p.Phe1810Val
|
|
XR_931024.1:n.200+937A>C
|
|
|
XR_931025.1:n.200+937A>C
|
|
|
XM_005253154.5:c.5542T>G
(SBF2)
|
XP_005253211.1:p.Phe1848Val
|
|
XM_005253155.5:c.5413T>G
(SBF2)
|
XP_005253212.1:p.Phe1805Val
|
|
XM_011520394.3:c.5428T>G
(SBF2)
|
XP_011518696.1:p.Phe1810Val
|
|
XM_017018372.2:c.5404T>G
(SBF2)
|
XP_016873861.1:p.Phe1802Val
|
|
XM_017018373.2:c.5404T>G
(SBF2)
|
XP_016873862.1:p.Phe1802Val
|
|
XM_017018374.2:c.5317T>G
(SBF2)
|
XP_016873863.1:p.Phe1773Val
|
|
XM_017018375.2:c.5305T>G
(SBF2)
|
XP_016873864.1:p.Phe1769Val
|
|
XR_001747994.2:n.5553T>G
(SBF2)
|
|
|
XR_001748470.1:n.200+937A>C
|
|
|
XR_001748471.1:n.85+937A>C
|
|
|
NM_001386339.1:c.5542T>G
(SBF2)
|
NP_001373268.1:p.Phe1848Val
|
|
NM_001386342.1:c.5317T>G
(SBF2)
|
NP_001373271.1:p.Phe1773Val
|
|
NM_030962.4:c.5446T>G
(SBF2)
MANE Select
|
NP_112224.1:p.Phe1816Val
|
|