|
ENST00000524961.6:n.799C>T
(SBF2)
|
|
|
|
ENST00000530741.2:c.2878C>T
(SBF2)
|
ENSP00000432643.2:p.Gln960Ter
|
|
|
ENST00000532095.2:n.851C>T
(SBF2)
|
|
|
|
ENST00000675281.2:c.4390C>T
(SBF2)
|
ENSP00000502491.1:p.Gln1464Ter
|
|
|
ENST00000676324.2:c.*623C>T
(SBF2)
|
ENSP00000502578.1:n.*623C>T
|
|
|
ENST00000676387.2:c.4372C>T
(SBF2)
|
ENSP00000502779.1:p.Gln1458Ter
|
|
|
ENST00000688344.1:c.3922C>T
(SBF2)
|
ENSP00000509987.1:p.Gln1308Ter
|
|
|
ENST00000689128.1:c.4411C>T
(SBF2)
|
ENSP00000509587.1:p.Gln1471Ter
|
|
|
ENST00000689258.1:c.4252C>T
(SBF2)
|
ENSP00000510475.1:p.Gln1418Ter
|
|
|
ENST00000689342.1:c.481C>T
(SBF2)
|
|
|
|
ENST00000689356.1:n.1486C>T
(SBF2)
|
|
|
|
ENST00000689597.1:c.3019C>T
(SBF2)
|
ENSP00000510781.1:p.Gln1007Ter
|
|
|
ENST00000689940.1:c.4309C>T
(SBF2)
|
ENSP00000508452.1:p.Gln1437Ter
|
|
|
ENST00000690944.1:c.522C>T
(SBF2)
|
|
|
|
ENST00000691616.1:n.791C>T
(SBF2)
|
|
|
|
ENST00000692716.1:c.4186C>T
(SBF2)
|
ENSP00000509545.1:p.Gln1396Ter
|
|
|
ENST00000693541.1:n.1234C>T
(SBF2)
|
|
|
|
ENST00000256190.13:c.4315C>T
(SBF2)
MANE Select
|
ENSP00000256190.8:p.Gln1439Ter
|
|
|
ENST00000675281.1:c.4390C>T
(SBF2)
|
ENSP00000502491.1:p.Gln1464Ter
|
|
|
ENST00000676324.1:c.*623C>T
(SBF2)
|
ENSP00000502578.1:n.*623C>T
|
|
|
ENST00000676387.1:c.4372C>T
(SBF2)
|
ENSP00000502779.1:p.Gln1458Ter
|
|
|
ENST00000256190.12:c.4315C>T
(SBF2)
|
ENSP00000256190.8:p.Gln1439Ter
|
|
|
ENST00000528478.1:n.383C>T
(SBF2)
|
|
|
|
ENST00000617179.4:c.4174C>T
(SBF2)
|
ENSP00000482806.1:p.Gln1392Ter
|
|
|
NM_030962.3:c.4315C>T , LRG_267t1:c.4315C>T
(SBF2)
|
NP_112224.1:p.Gln1439Ter
|
|
|
NR_036485.1:n.492G>A
(SBF2-AS1)
|
|
|
|
XM_005253154.3:c.4411C>T
(SBF2)
|
XP_005253211.1:p.Gln1471Ter
|
|
|
XM_005253155.3:c.4282C>T
(SBF2)
|
XP_005253212.1:p.Gln1428Ter
|
|
|
XM_011520394.1:c.4297C>T
(SBF2)
|
XP_011518696.1:p.Gln1433Ter
|
|
|
XM_005253154.5:c.4411C>T
(SBF2)
|
XP_005253211.1:p.Gln1471Ter
|
|
|
XM_005253155.5:c.4282C>T
(SBF2)
|
XP_005253212.1:p.Gln1428Ter
|
|
|
XM_011520394.3:c.4297C>T
(SBF2)
|
XP_011518696.1:p.Gln1433Ter
|
|
|
XM_017018372.2:c.4273C>T
(SBF2)
|
XP_016873861.1:p.Gln1425Ter
|
|
|
XM_017018373.2:c.4273C>T
(SBF2)
|
XP_016873862.1:p.Gln1425Ter
|
|
|
XM_017018374.2:c.4186C>T
(SBF2)
|
XP_016873863.1:p.Gln1396Ter
|
|
|
XM_017018375.2:c.4174C>T
(SBF2)
|
XP_016873864.1:p.Gln1392Ter
|
|
|
XR_001747994.2:n.4549C>T
(SBF2)
|
|
|
|
NM_001386339.1:c.4411C>T
(SBF2)
|
NP_001373268.1:p.Gln1471Ter
|
|
|
NM_001386342.1:c.4186C>T
(SBF2)
|
NP_001373271.1:p.Gln1396Ter
|
|
|
NM_030962.4:c.4315C>T
(SBF2)
MANE Select
|
NP_112224.1:p.Gln1439Ter
|
|
