ENST00000524961.6:n.2054C>G
(SBF2)
|
|
|
ENST00000675281.2:c.*20C>G
(SBF2)
|
ENSP00000502491.1:n.*20C>G
|
|
ENST00000676324.2:c.*1878C>G
(SBF2)
|
ENSP00000502578.1:n.*1878C>G
|
|
ENST00000676387.2:c.*20C>G
(SBF2)
|
ENSP00000502779.1:n.*20C>G
|
|
ENST00000688344.1:c.5177C>G
(SBF2)
|
ENSP00000509987.1:n.5177C>G
|
|
ENST00000689128.1:c.*20C>G
(SBF2)
|
ENSP00000509587.1:n.*20C>G
|
|
ENST00000689258.1:c.*20C>G
(SBF2)
|
ENSP00000510475.1:n.*20C>G
|
|
ENST00000689342.1:c.1736C>G
(SBF2)
|
|
|
ENST00000689356.1:n.2741C>G
(SBF2)
|
|
|
ENST00000689940.1:c.*20C>G
(SBF2)
|
ENSP00000508452.1:n.*20C>G
|
|
ENST00000690437.1:n.1519C>G
(SBF2)
|
|
|
ENST00000690944.1:c.1650C>G
(SBF2)
|
|
|
ENST00000691616.1:n.2046C>G
(SBF2)
|
|
|
ENST00000692716.1:c.*20C>G
(SBF2)
|
ENSP00000509545.1:n.*20C>G
|
|
ENST00000693541.1:n.2489C>G
(SBF2)
|
|
|
ENST00000256190.13:c.*20C>G
(SBF2)
MANE Select
|
ENSP00000256190.8:n.*20C>G
|
|
ENST00000675281.1:c.*20C>G
(SBF2)
|
ENSP00000502491.1:n.*20C>G
|
|
ENST00000676324.1:c.*1878C>G
(SBF2)
|
ENSP00000502578.1:n.*1878C>G
|
|
ENST00000676387.1:c.*20C>G
(SBF2)
|
ENSP00000502779.1:n.*20C>G
|
|
ENST00000256190.12:c.*20C>G
(SBF2)
|
ENSP00000256190.8:n.*20C>G
|
|
ENST00000525040.5:n.873C>G
(SBF2)
|
|
|
ENST00000617179.4:c.5429C>G
(SBF2)
|
ENSP00000482806.1:n.5429C>G
|
|
NM_030962.3:c.*20C>G , LRG_267t1:c.*20C>G
(SBF2)
|
NP_112224.1:n.*20C>G
|
|
NR_036485.1:n.211+21895G>C
(SBF2-AS1)
|
|
|
XM_005253154.3:c.*20C>G
(SBF2)
|
XP_005253211.1:n.*20C>G
|
|
XM_005253155.3:c.*20C>G
(SBF2)
|
XP_005253212.1:n.*20C>G
|
|
XM_011520394.1:c.*20C>G
(SBF2)
|
XP_011518696.1:n.*20C>G
|
|
XR_931024.1:n.23G>C
|
|
|
XR_931025.1:n.23G>C
|
|
|
XM_005253154.5:c.*20C>G
(SBF2)
|
XP_005253211.1:n.*20C>G
|
|
XM_005253155.5:c.*20C>G
(SBF2)
|
XP_005253212.1:n.*20C>G
|
|
XM_011520394.3:c.*20C>G
(SBF2)
|
XP_011518696.1:n.*20C>G
|
|
XM_017018372.2:c.*20C>G
(SBF2)
|
XP_016873861.1:n.*20C>G
|
|
XM_017018373.2:c.*20C>G
(SBF2)
|
XP_016873862.1:n.*20C>G
|
|
XM_017018374.2:c.*20C>G
(SBF2)
|
XP_016873863.1:n.*20C>G
|
|
XM_017018375.2:c.*20C>G
(SBF2)
|
XP_016873864.1:n.*20C>G
|
|
XR_001747994.2:n.5677C>G
(SBF2)
|
|
|
XR_001748470.1:n.23G>C
|
|
|
NM_001386339.1:c.*20C>G
(SBF2)
|
NP_001373268.1:n.*20C>G
|
|
NM_001386342.1:c.*20C>G
(SBF2)
|
NP_001373271.1:n.*20C>G
|
|
NM_030962.4:c.*20C>G
(SBF2)
MANE Select
|
NP_112224.1:n.*20C>G
|
|