ENST00000233627.14:c.410T>A
MANE Select
|
ENSP00000233627.9:p.Val137Asp
|
|
ENST00000233627.13:c.410T>A
|
ENSP00000233627.9:p.Val137Asp
|
|
ENST00000313408.11:c.410T>A
|
ENSP00000364262.5:p.Val137Asp
|
|
ENST00000414651.3:c.500T>A
|
ENSP00000406630.2:p.Val167Asp
|
|
ENST00000436115.6:n.2365T>A
|
|
|
ENST00000534853.5:c.*204T>A
|
ENSP00000442822.1:n.*204T>A
|
|
ENST00000535382.1:n.662T>A
|
|
|
ENST00000538523.5:n.466T>A
|
|
|
ENST00000538662.5:n.505T>A
|
|
|
ENST00000538929.5:n.500T>A
|
|
|
ENST00000539480.5:c.410T>A
|
ENSP00000443273.1:p.Val137Asp
|
|
ENST00000540530.5:n.401T>A
|
|
|
ENST00000543289.5:n.968T>A
|
|
|
ENST00000545446.5:n.701T>A
|
|
|
ENST00000546172.7:c.*406T>A
|
ENSP00000467094.1:n.*406T>A
|
|
ENST00000546283.5:c.410T>A
|
ENSP00000440348.1:p.Val137Asp
|
|
ENST00000618074.4:c.428-11T>A
|
ENSP00000477895.1:n.428-11T>A
|
|
ENST00000620479.4:c.415-1T>A
|
ENSP00000480984.1:n.415-1T>A
|
|
ENST00000622587.4:n.474T>A
|
|
|
NM_024407.4:c.410T>A
|
NP_077718.3:p.Val137Asp
|
|
XM_005259556.3:c.410T>A
|
XP_005259613.2:p.Val137Asp
|
|
NM_001363602.1:c.410T>A
|
NP_001350531.1:p.Val137Asp
|
|
XM_024451499.1:c.431T>A
|
XP_024307267.1:p.Val144Asp
|
|
NM_024407.5:c.410T>A
MANE Select
|
NP_077718.3:p.Val137Asp
|
|
NM_001363602.2:c.410T>A
|
NP_001350531.1:p.Val137Asp
|
|