ENST00000470094.2:c.9264C>A
|
ENSP00000434898.2:p.Ala3088=
|
|
ENST00000528762.2:c.*631C>A
|
ENSP00000433168.2:n.*631C>A
|
|
ENST00000530893.7:c.8895C>A
|
ENSP00000499438.2:p.Ala2965=
|
|
ENST00000665585.2:c.*826C>A
|
ENSP00000499570.2:n.*826C>A
|
|
ENST00000666593.2:c.*109C>A
|
ENSP00000499256.2:n.*109C>A
|
|
ENST00000700202.2:c.9213C>A
|
ENSP00000514856.2:p.Ala3071=
|
|
ENST00000700202.1:c.1680C>A
|
ENSP00000514856.1:p.Ala560=
|
|
ENST00000700203.1:n.1391C>A
|
|
|
ENST00000380152.8:c.9264C>A
MANE Select
|
ENSP00000369497.3:p.Ala3088=
|
|
ENST00000544455.6:c.9264C>A
|
ENSP00000439902.1:p.Ala3088=
|
|
ENST00000614259.2:c.9272C>A
|
ENSP00000506251.1:n.9272C>A
|
|
ENST00000665585.1:c.2142C>A
|
|
|
ENST00000666593.1:c.286C>A
|
ENSP00000499256.1:n.286C>A
|
|
ENST00000680887.1:c.9264C>A
|
ENSP00000505508.1:p.Ala3088=
|
|
ENST00000380152.7:c.9264C>A
|
ENSP00000369497.3:p.Ala3088=
|
|
ENST00000470094.1:c.221C>A
|
|
|
ENST00000544455.5:c.9264C>A
|
ENSP00000439902.1:p.Ala3088=
|
|
NM_000059.3:c.9264C>A , LRG_293t1:c.9264C>A
|
NP_000050.2:p.Ala3088=
|
|
XM_011535203.1:c.9264C>A
|
XP_011533505.1:p.Ala3088=
|
|
XM_011535204.1:c.9168C>A
|
XP_011533506.1:p.Ala3056=
|
|
NM_000059.4:c.9264C>A
MANE Select
|
NP_000050.3:p.Ala3088=
|
|