ENST00000222747.8:c.894A>G
MANE Select
|
ENSP00000222747.3:p.Thr298=
|
|
ENST00000222747.7:c.894A>G
|
ENSP00000222747.3:p.Thr298=
|
|
ENST00000415871.5:c.894A>G
|
ENSP00000397699.1:p.Thr298=
|
|
ENST00000450414.5:c.873A>G
|
ENSP00000397411.1:n.873A>G
|
|
NM_012338.3:c.894A>G
|
NP_036470.1:p.Thr298=
|
|
XM_005250239.1:c.894A>G
|
XP_005250296.1:p.Thr298=
|
|
XM_011515993.1:c.894A>G
|
XP_011514295.1:p.Thr298=
|
|
XM_011515994.1:c.894A>G
|
XP_011514296.1:p.Thr298=
|
|
XM_005250239.3:c.894A>G
|
XP_005250296.1:p.Thr298=
|
|
XM_017011913.1:c.819A>G
|
XP_016867402.1:p.Thr273=
|
|
NM_012338.4:c.894A>G
MANE Select
|
NP_036470.1:p.Thr298=
|
|