ENST00000696264.1:c.674A>T
|
ENSP00000512511.1:p.Glu225Val
|
|
ENST00000696265.1:c.674A>T
|
ENSP00000512512.1:p.Glu225Val
|
|
ENST00000696266.1:c.392A>T
|
ENSP00000512513.1:p.Glu131Val
|
|
ENST00000696267.1:n.314A>T
|
|
|
ENST00000229769.3:c.674A>T
MANE Select
|
ENSP00000229769.2:p.Glu225Val
|
|
ENST00000648059.1:c.674A>T
|
ENSP00000497902.1:p.Glu225Val
|
|
ENST00000229769.2:c.674A>T
|
ENSP00000229769.2:p.Glu225Val
|
|
NM_021922.2:c.674A>T , LRG_498t1:c.674A>T
|
NP_068741.1:p.Glu225Val
|
|
XM_005248885.2:c.674A>T
|
XP_005248942.1:p.Glu225Val
|
|
XM_005248886.2:c.674A>T
|
XP_005248943.1:p.Glu225Val
|
|
XM_005248887.2:c.674A>T
|
XP_005248944.1:p.Glu225Val
|
|
XM_005248888.2:c.674A>T
|
XP_005248945.1:p.Glu225Val
|
|
XM_011514343.1:c.380A>T
|
XP_011512645.1:p.Glu127Val
|
|
XM_011514344.1:c.380A>T
|
XP_011512646.1:p.Glu127Val
|
|
XM_005248888.3:c.674A>T
|
XP_005248945.1:p.Glu225Val
|
|
XM_011514343.2:c.380A>T
|
XP_011512645.1:p.Glu127Val
|
|
XR_001743226.1:n.881A>T
|
|
|
XR_002956267.1:n.881A>T
|
|
|
NM_021922.3:c.674A>T
MANE Select
|
NP_068741.1:p.Glu225Val
|
|