|
ENST00000478464.6:c.569A>T
|
ENSP00000419303.2:p.Asp190Val
|
|
|
ENST00000480644.2:c.695A>T
|
ENSP00000420229.2:p.Asp232Val
|
|
|
ENST00000492644.2:n.3033A>T
|
|
|
|
ENST00000684961.1:c.398A>T
|
ENSP00000508439.1:p.Asp133Val
|
|
|
ENST00000686433.1:c.725A>T
|
ENSP00000509173.1:p.Asp242Val
|
|
|
ENST00000687538.1:c.569A>T
|
ENSP00000508887.1:p.Asp190Val
|
|
|
ENST00000688697.1:c.779A>T
|
ENSP00000510396.1:p.Asp260Val
|
|
|
ENST00000689286.1:c.569A>T
|
ENSP00000509897.1:p.Asp190Val
|
|
|
ENST00000689925.1:c.*120A>T
|
ENSP00000510082.1:n.*120A>T
|
|
|
ENST00000690298.1:c.*420A>T
|
ENSP00000509376.1:n.*420A>T
|
|
|
ENST00000691070.1:c.695A>T
|
ENSP00000509723.1:p.Asp232Val
|
|
|
ENST00000692727.1:n.3301A>T
|
|
|
|
ENST00000693155.1:n.1456A>T
|
|
|
|
ENST00000310776.9:c.776A>T
|
ENSP00000310785.5:p.Asp259Val
|
|
|
ENST00000680020.1:c.779A>T
MANE Select
|
ENSP00000505414.1:p.Asp260Val
|
|
|
ENST00000310776.8:c.779A>T
|
ENSP00000310785.4:p.Asp260Val
|
|
|
ENST00000465056.5:c.776A>T
|
ENSP00000418233.1:p.Asp259Val
|
|
|
ENST00000478464.5:c.656A>T
|
ENSP00000419303.1:p.Asp219Val
|
|
|
ENST00000480644.1:c.264A>T
|
|
|
|
ENST00000480938.5:n.1433A>T
|
|
|
|
ENST00000492644.1:n.1824A>T
|
|
|
|
ENST00000495075.5:c.779A>T
|
ENSP00000418008.1:p.Asp260Val
|
|
|
ENST00000498505.5:c.*376A>T
|
ENSP00000420482.1:n.*376A>T
|
|
|
NM_020191.2:c.779A>T
|
NP_064576.1:p.Asp260Val
|
|
|
XM_005247640.2:c.776A>T
|
XP_005247697.1:p.Asp259Val
|
|
|
XM_006713703.2:c.725A>T
|
XP_006713766.1:p.Asp242Val
|
|
|
XM_011512995.1:c.656A>T
|
XP_011511297.1:p.Asp219Val
|
|
|
XM_011512996.1:c.653A>T
|
XP_011511298.1:p.Asp218Val
|
|
|
NM_001363857.1:c.656A>T
|
NP_001350786.1:p.Asp219Val
|
|
|
NM_001363893.1:c.776A>T
|
NP_001350822.1:p.Asp259Val
|
|
|
NM_020191.3:c.779A>T
|
NP_064576.1:p.Asp260Val
|
|
|
XM_006713703.4:c.725A>T
|
XP_006713766.1:p.Asp242Val
|
|
|
XM_011512996.2:c.653A>T
|
XP_011511298.1:p.Asp218Val
|
|
|
NM_020191.4:c.779A>T
MANE Select
|
NP_064576.1:p.Asp260Val
|
|
