ENST00000395796.8:c.*392G>A
|
ENSP00000379142.4:n.*392G>A
|
|
ENST00000616242.5:c.394G>A
|
ENSP00000482149.2:p.Asp132Asn
|
|
ENST00000682635.1:n.880G>A
|
|
|
ENST00000345378.7:c.397G>A
|
ENSP00000223366.2:p.Asp133Asn
|
|
ENST00000403799.8:c.394G>A
MANE Select
|
ENSP00000384247.3:p.Asp132Asn
|
|
ENST00000671824.1:c.394G>A
|
ENSP00000500264.1:p.Asp132Asn
|
|
ENST00000673284.1:c.394G>A
|
ENSP00000499852.1:p.Asp132Asn
|
|
ENST00000345378.6:c.397G>A
|
ENSP00000223366.2:p.Asp133Asn
|
|
ENST00000395796.7:c.391G>A
|
ENSP00000379142.3:p.Asp131Asn
|
|
ENST00000403799.7:c.394G>A
|
ENSP00000384247.3:p.Asp132Asn
|
|
ENST00000437084.1:c.364-21G>A
|
ENSP00000402840.1:n.364-21G>A
|
|
ENST00000616242.4:c.391G>A
|
ENSP00000482149.1:p.Asp131Asn
|
|
NM_000162.3:c.394G>A
|
NP_000153.1:p.Asp132Asn
|
|
NM_033507.1:c.397G>A
|
NP_277042.1:p.Asp133Asn
|
|
NM_033508.1:c.391G>A
|
NP_277043.1:p.Asp131Asn
|
|
NM_000162.4:c.394G>A
|
NP_000153.1:p.Asp132Asn
|
|
NM_001354800.1:c.394G>A
|
NP_001341729.1:p.Asp132Asn
|
|
NM_033507.2:c.397G>A
|
NP_277042.1:p.Asp133Asn
|
|
NM_033508.2:c.391G>A
|
NP_277043.1:p.Asp131Asn
|
|
NM_000162.5:c.394G>A
MANE Select
|
NP_000153.1:p.Asp132Asn
|
|
NM_033507.3:c.397G>A
|
NP_277042.1:p.Asp133Asn
|
|
NM_033508.3:c.391G>A
|
NP_277043.1:p.Asp131Asn
|
|