ENST00000426508.7:c.2678A>T
MANE Select
|
ENSP00000406012.2:p.Glu893Val
|
|
ENST00000361339.9:c.260A>T
|
ENSP00000354895.5:p.Glu87Val
|
|
ENST00000397417.6:c.*1116A>T
|
ENSP00000380562.2:n.*1116A>T
|
|
ENST00000426508.6:c.2678A>T
|
ENSP00000406012.2:p.Glu893Val
|
|
ENST00000565298.5:n.1907A>T
|
|
|
ENST00000566818.1:n.393A>T
|
|
|
NM_014714.3:c.2678A>T
|
NP_055529.2:p.Glu893Val
|
|
XM_006720989.2:c.2678A>T
|
XP_006721052.1:p.Glu893Val
|
|
XM_006720990.2:c.2678A>T
|
XP_006721053.1:p.Glu893Val
|
|
XM_006720991.2:c.2678A>T
|
XP_006721054.1:p.Glu893Val
|
|
XM_006720992.2:c.311A>T
|
XP_006721055.1:p.Glu104Val
|
|
XM_011522766.1:c.2432A>T
|
XP_011521068.1:p.Glu811Val
|
|
XM_011522767.1:c.1703A>T
|
XP_011521069.1:p.Glu568Val
|
|
XM_006720990.3:c.2678A>T
|
XP_006721053.1:p.Glu893Val
|
|
XM_006720991.3:c.2678A>T
|
XP_006721054.1:p.Glu893Val
|
|
XM_006720992.3:c.311A>T
|
XP_006721055.1:p.Glu104Val
|
|
XM_011522766.3:c.2432A>T
|
XP_011521068.1:p.Glu811Val
|
|
XM_011522767.2:c.1703A>T
|
XP_011521069.1:p.Glu568Val
|
|
XM_017023910.1:c.2678A>T
|
XP_016879399.1:p.Glu893Val
|
|
XM_017023911.1:c.863A>T
|
XP_016879400.1:p.Glu288Val
|
|
NM_014714.4:c.2678A>T
MANE Select
|
NP_055529.2:p.Glu893Val
|
|