ENST00000456935.7:c.2754G>A
MANE Select
|
ENSP00000395473.2:p.Glu918=
|
|
ENST00000221363.8:c.2751G>A
|
ENSP00000221363.4:p.Glu917=
|
|
ENST00000456935.6:c.2754G>A
|
ENSP00000395473.2:p.Glu918=
|
|
ENST00000466794.5:n.3344G>A
|
|
|
ENST00000469423.1:n.76G>A
|
|
|
ENST00000493218.5:n.165G>A
|
|
|
ENST00000597692.1:c.313G>A
|
|
|
NM_000528.3:c.2754G>A
|
NP_000519.2:p.Glu918=
|
|
NM_001173498.1:c.2751G>A
|
NP_001166969.1:p.Glu917=
|
|
XM_005259913.1:c.2757G>A
|
XP_005259970.1:p.Glu919=
|
|
XM_011528017.1:c.1653G>A
|
XP_011526319.1:p.Glu551=
|
|
XM_005259913.2:c.2757G>A
|
XP_005259970.1:p.Glu919=
|
|
XM_024451518.1:c.1653G>A
|
XP_024307286.1:p.Glu551=
|
|
NM_000528.4:c.2754G>A
MANE Select
|
NP_000519.2:p.Glu918=
|
|
NM_001173498.2:c.2751G>A
|
NP_001166969.1:p.Glu917=
|
|