|
ENST00000524961.6:n.1244C>G
(SBF2)
|
|
|
|
ENST00000532095.2:n.1296C>G
(SBF2)
|
|
|
|
ENST00000675281.2:c.4835C>G
(SBF2)
|
ENSP00000502491.1:p.Thr1612Ser
|
|
|
ENST00000676324.2:c.*1068C>G
(SBF2)
|
ENSP00000502578.1:n.*1068C>G
|
|
|
ENST00000676387.2:c.4817C>G
(SBF2)
|
ENSP00000502779.1:p.Thr1606Ser
|
|
|
ENST00000688344.1:c.4367C>G
(SBF2)
|
ENSP00000509987.1:p.Thr1456Ser
|
|
|
ENST00000689128.1:c.4856C>G
(SBF2)
|
ENSP00000509587.1:p.Thr1619Ser
|
|
|
ENST00000689258.1:c.4697C>G
(SBF2)
|
ENSP00000510475.1:p.Thr1566Ser
|
|
|
ENST00000689342.1:c.926C>G
(SBF2)
|
|
|
|
ENST00000689356.1:n.1931C>G
(SBF2)
|
|
|
|
ENST00000689597.1:c.3464C>G
(SBF2)
|
ENSP00000510781.1:p.Thr1155Ser
|
|
|
ENST00000689940.1:c.4754C>G
(SBF2)
|
ENSP00000508452.1:p.Thr1585Ser
|
|
|
ENST00000690944.1:c.840C>G
(SBF2)
|
|
|
|
ENST00000691616.1:n.1236C>G
(SBF2)
|
|
|
|
ENST00000692716.1:c.4631C>G
(SBF2)
|
ENSP00000509545.1:p.Thr1544Ser
|
|
|
ENST00000693541.1:n.1679C>G
(SBF2)
|
|
|
|
ENST00000256190.13:c.4760C>G
(SBF2)
MANE Select
|
ENSP00000256190.8:p.Thr1587Ser
|
|
|
ENST00000675281.1:c.4835C>G
(SBF2)
|
ENSP00000502491.1:p.Thr1612Ser
|
|
|
ENST00000676324.1:c.*1068C>G
(SBF2)
|
ENSP00000502578.1:n.*1068C>G
|
|
|
ENST00000676387.1:c.4817C>G
(SBF2)
|
ENSP00000502779.1:p.Thr1606Ser
|
|
|
ENST00000256190.12:c.4760C>G
(SBF2)
|
ENSP00000256190.8:p.Thr1587Ser
|
|
|
ENST00000617179.4:c.4619C>G
(SBF2)
|
ENSP00000482806.1:p.Thr1540Ser
|
|
|
NM_030962.3:c.4760C>G , LRG_267t1:c.4760C>G
(SBF2)
|
NP_112224.1:p.Thr1587Ser
|
|
|
NR_036485.1:n.212-18567G>C
(SBF2-AS1)
|
|
|
|
XM_005253154.3:c.4856C>G
(SBF2)
|
XP_005253211.1:p.Thr1619Ser
|
|
|
XM_005253155.3:c.4727C>G
(SBF2)
|
XP_005253212.1:p.Thr1576Ser
|
|
|
XM_011520394.1:c.4742C>G
(SBF2)
|
XP_011518696.1:p.Thr1581Ser
|
|
|
XR_931024.1:n.456-1588G>C
|
|
|
|
XR_931025.1:n.271-1588G>C
|
|
|
|
XM_005253154.5:c.4856C>G
(SBF2)
|
XP_005253211.1:p.Thr1619Ser
|
|
|
XM_005253155.5:c.4727C>G
(SBF2)
|
XP_005253212.1:p.Thr1576Ser
|
|
|
XM_011520394.3:c.4742C>G
(SBF2)
|
XP_011518696.1:p.Thr1581Ser
|
|
|
XM_017018372.2:c.4718C>G
(SBF2)
|
XP_016873861.1:p.Thr1573Ser
|
|
|
XM_017018373.2:c.4718C>G
(SBF2)
|
XP_016873862.1:p.Thr1573Ser
|
|
|
XM_017018374.2:c.4631C>G
(SBF2)
|
XP_016873863.1:p.Thr1544Ser
|
|
|
XM_017018375.2:c.4619C>G
(SBF2)
|
XP_016873864.1:p.Thr1540Ser
|
|
|
XR_001747994.2:n.4867C>G
(SBF2)
|
|
|
|
NM_001386339.1:c.4856C>G
(SBF2)
|
NP_001373268.1:p.Thr1619Ser
|
|
|
NM_001386342.1:c.4631C>G
(SBF2)
|
NP_001373271.1:p.Thr1544Ser
|
|
|
NM_030962.4:c.4760C>G
(SBF2)
MANE Select
|
NP_112224.1:p.Thr1587Ser
|
|
