ENST00000333213.11:c.966G>T
MANE Select
|
ENSP00000327487.6:p.Leu322=
|
|
ENST00000434205.8:c.663G>T
|
ENSP00000406559.4:p.Leu221=
|
|
ENST00000545228.3:c.966G>T
|
ENSP00000438169.3:p.Leu322=
|
|
ENST00000579449.2:n.765G>T
|
|
|
ENST00000580013.6:n.1169G>T
|
|
|
ENST00000679370.1:n.1547G>T
|
|
|
ENST00000679429.1:c.*424G>T
|
ENSP00000505403.1:n.*424G>T
|
|
ENST00000679443.1:n.1035G>T
|
|
|
ENST00000679782.1:c.966G>T
|
ENSP00000505995.1:p.Leu322=
|
|
ENST00000679919.1:n.1035G>T
|
|
|
ENST00000679928.1:c.*577G>T
|
ENSP00000506071.1:n.*577G>T
|
|
ENST00000680528.1:n.991G>T
|
|
|
ENST00000680999.1:c.966G>T
|
ENSP00000504984.1:p.Leu322=
|
|
ENST00000681282.1:c.*212G>T
|
ENSP00000506339.1:n.*212G>T
|
|
ENST00000333213.10:c.966G>T
|
ENSP00000327487.6:p.Leu322=
|
|
ENST00000545228.2:c.55G>T
|
|
|
ENST00000578415.1:c.926G>T
|
|
|
ENST00000583173.5:c.499G>T
|
ENSP00000463619.1:p.Ala167Ser
|
|
NM_207346.2:c.966G>T
|
NP_997229.2:p.Leu322=
|
|
XM_005257229.2:c.966G>T
|
XP_005257286.1:p.Leu322=
|
|
XM_006721821.2:c.663G>T
|
XP_006721884.1:p.Leu221=
|
|
XM_011524616.1:c.966G>T
|
XP_011522918.1:p.Leu322=
|
|
XM_011524617.1:c.966G>T
|
XP_011522919.1:p.Leu322=
|
|
XM_011524618.1:c.966G>T
|
XP_011522920.1:p.Leu322=
|
|
XR_243646.2:n.996G>T
|
|
|
XM_005257229.4:c.966G>T
|
XP_005257286.1:p.Leu322=
|
|
XR_243646.4:n.1002G>T
|
|
|
NM_207346.3:c.966G>T
MANE Select
|
NP_997229.2:p.Leu322=
|
|