ENST00000222747.8:c.832C=
MANE Select
|
ENSP00000222747.3:p.Leu278=
|
|
ENST00000222747.7:c.832C=
|
ENSP00000222747.3:p.Leu278=
|
|
ENST00000415871.5:c.832C=
|
ENSP00000397699.1:p.Leu278=
|
|
ENST00000450414.5:c.811C=
|
ENSP00000397411.1:n.811C=
|
|
NM_012338.3:c.832C=
|
NP_036470.1:p.Leu278=
|
|
XM_005250239.1:c.832C=
|
XP_005250296.1:p.Leu278=
|
|
XM_011515993.1:c.832C=
|
XP_011514295.1:p.Leu278=
|
|
XM_011515994.1:c.832C=
|
XP_011514296.1:p.Leu278=
|
|
XM_005250239.3:c.832C=
|
XP_005250296.1:p.Leu278=
|
|
XM_017011913.1:c.757C=
|
XP_016867402.1:p.Leu253=
|
|
NM_012338.4:c.832C=
MANE Select
|
NP_036470.1:p.Leu278=
|
|