ENST00000274695.8:c.372-11278C=
MANE Select
|
ENSP00000274695.4:n.372-11278C=
|
|
ENST00000378610.1:c.372-11278C=
|
ENSP00000367873.1:n.372-11278C=
|
|
NM_017774.3:c.372-11278C=
MANE Select
|
NP_060244.2:n.372-11278C=
|
|
XM_006715128.2:c.372-11278C=
|
XP_006715191.1:n.372-11278C=
|
|
XM_011514718.1:c.372-11278C=
|
XP_011513020.1:n.372-11278C=
|
|
XM_011514719.1:c.372-11278C=
|
XP_011513021.1:n.372-11278C=
|
|
XR_926265.1:n.539-11278C=
|
|
|
XR_926266.1:n.652-11278C=
|
|
|
XR_926267.1:n.539-11278C=
|
|
|
XM_011514719.2:c.372-11278C=
|
XP_011513021.1:n.372-11278C=
|
|
XM_017010986.1:c.372-11278C=
|
XP_016866475.1:n.372-11278C=
|
|
XM_017010987.1:c.-383-11278C=
|
XP_016866476.1:n.-383-11278C=
|
|
XM_024446481.1:c.372-11278C=
|
XP_024302249.1:n.372-11278C=
|
|
XR_001743495.2:n.544-11278C=
|
|
|
XR_001743496.2:n.939-11278C=
|
|
|
XR_001743500.1:n.539-11278C=
|
|
|
XR_001743501.1:n.539-11278C=
|
|
|
XR_926265.2:n.539-11278C=
|
|
|
XR_926266.2:n.652-11278C=
|
|
|
XR_926267.2:n.539-11278C=
|
|
|