ENST00000524470.2:c.*662G>A
|
ENSP00000514307.1:n.*662G>A
|
|
ENST00000525976.6:c.2313G>A
|
ENSP00000434831.2:p.Glu771=
|
|
ENST00000527481.3:c.2313G>A
|
ENSP00000466340.2:p.Glu771=
|
|
ENST00000529370.6:n.2644G>A
|
|
|
ENST00000529739.2:n.2727G>A
|
|
|
ENST00000530829.2:c.*1864G>A
|
ENSP00000436826.2:n.*1864G>A
|
|
ENST00000531836.6:c.2313G>A
|
ENSP00000436175.2:p.Glu771=
|
|
ENST00000533334.2:c.*355G>A
|
ENSP00000432320.2:n.*355G>A
|
|
ENST00000534228.2:n.2727G>A
|
|
|
ENST00000699354.1:n.415G>A
|
|
|
ENST00000699355.1:c.*373G>A
|
ENSP00000514328.1:n.*373G>A
|
|
ENST00000699356.1:n.2727G>A
|
|
|
ENST00000699357.1:n.2727G>A
|
|
|
ENST00000699358.1:c.2313G>A
|
ENSP00000514329.1:p.Glu771=
|
|
ENST00000699360.1:c.2313G>A
|
ENSP00000514331.1:p.Glu771=
|
|
ENST00000525621.6:c.2313G>A
MANE Select
|
ENSP00000431885.1:p.Glu771=
|
|
ENST00000264818.10:c.2313G>A
|
ENSP00000264818.6:p.Glu771=
|
|
ENST00000524462.5:c.1758G>A
|
ENSP00000433203.1:p.Glu586=
|
|
ENST00000525621.5:c.2313G>A
|
ENSP00000431885.1:p.Glu771=
|
|
ENST00000529370.5:c.2313G>A
|
ENSP00000432728.1:p.Glu771=
|
|
ENST00000533334.1:c.602G>A
|
|
|
NM_003331.4:c.2313G>A , LRG_121t1:c.2313G>A
|
NP_003322.3:p.Glu771=
|
|
XM_011528245.1:c.2313G>A
|
XP_011526547.1:p.Glu771=
|
|
XM_011528246.1:c.2016G>A
|
XP_011526548.1:p.Glu672=
|
|
XM_011528247.1:c.2016G>A
|
XP_011526549.1:p.Glu672=
|
|
XM_011528248.1:c.2313G>A
|
XP_011526550.1:p.Glu771=
|
|
XM_011528249.1:c.987G>A
|
XP_011526551.1:p.Glu329=
|
|
XM_011528251.1:c.570G>A
|
XP_011526553.1:p.Glu190=
|
|
XM_011528246.3:c.2016G>A
|
XP_011526548.1:p.Glu672=
|
|
XM_011528249.2:c.987G>A
|
XP_011526551.1:p.Glu329=
|
|
XR_001753750.1:n.2470G>A
|
|
|
XR_001753751.1:n.2470G>A
|
|
|
XR_001753752.1:n.2582G>A
|
|
|
XR_002958353.1:n.2351G>A
|
|
|
NM_003331.5:c.2313G>A
MANE Select
|
NP_003322.3:p.Glu771=
|
|
NM_001385197.1:c.2313G>A
|
NP_001372126.1:p.Glu771=
|
|
NM_001385198.1:c.2313G>A
|
NP_001372127.1:p.Glu771=
|
|
NM_001385199.1:c.2127G>A
|
NP_001372128.1:p.Glu709=
|
|
NM_001385200.1:c.2313G>A
|
NP_001372129.1:p.Glu771=
|
|
NM_001385201.1:c.2115G>A
|
NP_001372130.1:p.Glu705=
|
|
NM_001385202.1:c.2229G>A
|
NP_001372131.1:p.Glu743=
|
|
NM_001385203.1:c.2313G>A
|
NP_001372132.1:p.Glu771=
|
|
NM_001385204.1:c.2313G>A
|
NP_001372133.1:p.Glu771=
|
|
NM_001385205.1:c.2223G>A
|
NP_001372134.1:p.Glu741=
|
|
NM_001385206.1:c.2187G>A
|
NP_001372135.1:p.Glu729=
|
|
NM_001385207.1:c.2295G>A
|
NP_001372136.1:p.Glu765=
|
|