ENST00000286621.7:c.615A>C
|
ENSP00000286621.3:p.Glu205Asp
|
|
ENST00000372734.5:c.564A>C
|
ENSP00000361819.3:p.Glu188Asp
|
|
ENST00000539909.6:c.615A>C
MANE Select
|
ENSP00000443965.2:p.Glu205Asp
|
|
ENST00000541550.6:c.564A>C
|
ENSP00000438321.2:p.Glu188Asp
|
|
ENST00000672394.1:c.339A>C
|
ENSP00000500390.1:p.Glu113Asp
|
|
ENST00000672429.1:c.556-63967A>C
|
ENSP00000500292.1:n.556-63967A>C
|
|
ENST00000672604.1:c.355A>C
|
|
|
ENST00000672920.1:c.*360A>C
|
ENSP00000500141.1:n.*360A>C
|
|
ENST00000673027.1:c.510A>C
|
ENSP00000500201.1:p.Glu170Asp
|
|
ENST00000673310.1:c.564A>C
|
ENSP00000500097.1:p.Glu188Asp
|
|
ENST00000673352.1:c.615A>C
|
ENSP00000500056.1:p.Glu205Asp
|
|
ENST00000286621.6:c.615A>C
|
ENSP00000286621.2:p.Glu205Asp
|
|
ENST00000372734.3:c.564A>C
|
ENSP00000361819.3:p.Glu188Asp
|
|
ENST00000539909.5:c.556-63967A>C
|
ENSP00000443965.1:n.556-63967A>C
|
|
ENST00000541550.5:c.510A>C
|
ENSP00000438321.1:p.Glu170Asp
|
|
NM_001123.3:c.564A>C
|
NP_001114.2:p.Glu188Asp
|
|
NM_001202449.1:c.510A>C
|
NP_001189378.1:p.Glu170Asp
|
|
NM_001202450.1:c.556-63967A>C
|
NP_001189379.1:n.556-63967A>C
|
|
NM_006721.3:c.615A>C
|
NP_006712.2:p.Glu205Asp
|
|
NR_120673.1:n.259+2451T>G
|
|
|
XM_011539297.1:c.531A>C
|
XP_011537599.1:p.Glu177Asp
|
|
XM_017015698.1:c.615A>C
|
XP_016871187.1:p.Glu205Asp
|
|
XM_017015699.1:c.420A>C
|
XP_016871188.1:p.Glu140Asp
|
|
XM_017015700.1:c.615A>C
|
XP_016871189.1:p.Glu205Asp
|
|
XM_017015701.1:c.505-63967A>C
|
XP_016871190.1:n.505-63967A>C
|
|
XM_017015702.1:c.564A>C
|
XP_016871191.1:p.Glu188Asp
|
|
XM_017015703.2:c.339A>C
|
XP_016871192.1:p.Glu113Asp
|
|
XM_017015704.1:c.615A>C
|
XP_016871193.1:p.Glu205Asp
|
|
XM_017015705.1:c.556-63967A>C
|
XP_016871194.1:n.556-63967A>C
|
|
XM_017015706.1:c.564A>C
|
XP_016871195.1:p.Glu188Asp
|
|
NM_001369123.1:c.615A>C
|
NP_001356052.1:p.Glu205Asp
|
|
NM_001369124.1:c.505-63967A>C
|
NP_001356053.1:n.505-63967A>C
|
|
NM_006721.4:c.615A>C
MANE Select
|
NP_006712.2:p.Glu205Asp
|
|
NM_001123.4:c.564A>C
|
NP_001114.2:p.Glu188Asp
|
|
NM_001202449.2:c.510A>C
|
NP_001189378.1:p.Glu170Asp
|
|
NM_001202450.2:c.556-63967A>C
|
NP_001189379.1:n.556-63967A>C
|
|