ENST00000395796.8:c.*661G>T
|
ENSP00000379142.4:n.*661G>T
|
|
ENST00000616242.5:c.663G>T
|
ENSP00000482149.2:p.Glu221Asp
|
|
ENST00000682635.1:n.1149G>T
|
|
|
ENST00000345378.7:c.666G>T
|
ENSP00000223366.2:p.Glu222Asp
|
|
ENST00000403799.8:c.663G>T
MANE Select
|
ENSP00000384247.3:p.Glu221Asp
|
|
ENST00000671824.1:c.663G>T
|
ENSP00000500264.1:p.Glu221Asp
|
|
ENST00000673284.1:c.663G>T
|
ENSP00000499852.1:p.Glu221Asp
|
|
ENST00000345378.6:c.666G>T
|
ENSP00000223366.2:p.Glu222Asp
|
|
ENST00000395796.7:c.660G>T
|
ENSP00000379142.3:p.Glu220Asp
|
|
ENST00000403799.7:c.663G>T
|
ENSP00000384247.3:p.Glu221Asp
|
|
ENST00000437084.1:c.612G>T
|
ENSP00000402840.1:p.Glu204Asp
|
|
ENST00000616242.4:c.660G>T
|
ENSP00000482149.1:p.Glu220Asp
|
|
NM_000162.3:c.663G>T
|
NP_000153.1:p.Glu221Asp
|
|
NM_033507.1:c.666G>T
|
NP_277042.1:p.Glu222Asp
|
|
NM_033508.1:c.660G>T
|
NP_277043.1:p.Glu220Asp
|
|
NM_000162.4:c.663G>T
|
NP_000153.1:p.Glu221Asp
|
|
NM_001354800.1:c.663G>T
|
NP_001341729.1:p.Glu221Asp
|
|
NM_033507.2:c.666G>T
|
NP_277042.1:p.Glu222Asp
|
|
NM_033508.2:c.660G>T
|
NP_277043.1:p.Glu220Asp
|
|
NM_000162.5:c.663G>T
MANE Select
|
NP_000153.1:p.Glu221Asp
|
|
NM_033507.3:c.666G>T
|
NP_277042.1:p.Glu222Asp
|
|
NM_033508.3:c.660G>T
|
NP_277043.1:p.Glu220Asp
|
|