ENST00000382103.7:c.1019A>T
MANE Select
|
ENSP00000371535.2:p.Glu340Val
|
|
ENST00000680581.1:c.1019A>T
|
ENSP00000506483.1:p.Glu340Val
|
|
ENST00000680824.1:n.2235A>T
|
|
|
ENST00000681071.1:n.1311A>T
|
|
|
ENST00000681341.1:n.2160A>T
|
|
|
ENST00000681948.1:c.1274A>T
|
ENSP00000505991.1:p.Glu425Val
|
|
ENST00000358971.7:c.*817A>T
|
ENSP00000351857.3:n.*817A>T
|
|
ENST00000382103.6:c.1019A>T
|
ENSP00000371535.2:p.Glu340Val
|
|
ENST00000503150.1:c.301A>T
|
|
|
ENST00000505513.1:n.319A>T
|
|
|
ENST00000514585.5:c.*720A>T
|
ENSP00000421880.1:n.*720A>T
|
|
NM_016955.3:c.1019A>T
|
NP_058651.3:p.Glu340Val
|
|
XM_005248168.2:c.782A>T
|
XP_005248225.1:p.Glu261Val
|
|
XM_006713965.2:c.839A>T
|
XP_006714028.1:p.Glu280Val
|
|
XM_011513846.1:c.1016A>T
|
XP_011512148.1:p.Glu339Val
|
|
XM_011513847.1:c.986A>T
|
XP_011512149.1:p.Glu329Val
|
|
XM_011513848.1:c.839A>T
|
XP_011512150.1:p.Glu280Val
|
|
XM_011513846.2:c.1016A>T
|
XP_011512148.1:p.Glu339Val
|
|
XM_011513847.2:c.986A>T
|
XP_011512149.1:p.Glu329Val
|
|
XM_017008277.1:c.1274A>T
|
XP_016863766.1:p.Glu425Val
|
|
XM_017008278.1:c.596A>T
|
XP_016863767.1:p.Glu199Val
|
|
NM_016955.4:c.1019A>T
MANE Select
|
NP_058651.3:p.Glu340Val
|
|