ENST00000530741.2:c.2340G=
|
ENSP00000432643.2:p.Gln780=
|
|
ENST00000675281.2:c.3636G=
|
ENSP00000502491.1:p.Gln1212=
|
|
ENST00000676324.2:c.3636G=
|
ENSP00000502578.1:p.Gln1212=
|
|
ENST00000676387.2:c.3522G=
|
ENSP00000502779.1:p.Gln1174=
|
|
ENST00000688344.1:c.3243G=
|
ENSP00000509987.1:p.Gln1081=
|
|
ENST00000689128.1:c.3636G=
|
ENSP00000509587.1:p.Gln1212=
|
|
ENST00000689258.1:c.3498G=
|
ENSP00000510475.1:p.Gln1166=
|
|
ENST00000689356.1:n.807G=
|
|
|
ENST00000689597.1:c.2340G=
|
ENSP00000510781.1:p.Gln780=
|
|
ENST00000689674.1:c.2530G=
|
ENSP00000510723.1:n.2530G=
|
|
ENST00000689940.1:c.3630G=
|
ENSP00000508452.1:p.Gln1210=
|
|
ENST00000690003.1:c.2435G=
|
ENSP00000508748.1:n.2435G=
|
|
ENST00000692716.1:c.3507G=
|
ENSP00000509545.1:p.Gln1169=
|
|
ENST00000693181.1:c.2465G=
|
ENSP00000510179.1:n.2465G=
|
|
ENST00000256190.13:c.3636G=
MANE Select
|
ENSP00000256190.8:p.Gln1212=
|
|
ENST00000675281.1:c.3636G=
|
ENSP00000502491.1:p.Gln1212=
|
|
ENST00000676324.1:c.3636G=
|
ENSP00000502578.1:p.Gln1212=
|
|
ENST00000676387.1:c.3522G=
|
ENSP00000502779.1:p.Gln1174=
|
|
ENST00000256190.12:c.3636G=
|
ENSP00000256190.8:p.Gln1212=
|
|
ENST00000530741.1:c.287G=
|
|
|
ENST00000617179.4:c.3495G=
|
ENSP00000482806.1:p.Gln1165=
|
|
NM_030962.3:c.3636G= , LRG_267t1:c.3636G=
|
NP_112224.1:p.Gln1212=
|
|
XM_005253154.3:c.3636G=
|
XP_005253211.1:p.Gln1212=
|
|
XM_005253155.3:c.3507G=
|
XP_005253212.1:p.Gln1169=
|
|
XM_011520394.1:c.3522G=
|
XP_011518696.1:p.Gln1174=
|
|
XM_011520395.1:c.3636G=
|
XP_011518697.1:p.Gln1212=
|
|
XM_005253154.5:c.3636G=
|
XP_005253211.1:p.Gln1212=
|
|
XM_005253155.5:c.3507G=
|
XP_005253212.1:p.Gln1169=
|
|
XM_011520394.3:c.3522G=
|
XP_011518696.1:p.Gln1174=
|
|
XM_011520395.3:c.3636G=
|
XP_011518697.1:p.Gln1212=
|
|
XM_017018372.2:c.3498G=
|
XP_016873861.1:p.Gln1166=
|
|
XM_017018373.2:c.3498G=
|
XP_016873862.1:p.Gln1166=
|
|
XM_017018374.2:c.3507G=
|
XP_016873863.1:p.Gln1169=
|
|
XM_017018375.2:c.3636G=
|
XP_016873864.1:p.Gln1212=
|
|
XM_017018376.2:c.3636G=
|
XP_016873865.1:p.Gln1212=
|
|
XR_001747994.2:n.3774G=
|
|
|
NM_001386339.1:c.3636G=
|
NP_001373268.1:p.Gln1212=
|
|
NM_001386342.1:c.3507G=
|
NP_001373271.1:p.Gln1169=
|
|
NM_030962.4:c.3636G=
MANE Select
|
NP_112224.1:p.Gln1212=
|
|