ENST00000395796.8:c.*982A>T
|
ENSP00000379142.4:n.*982A>T
|
|
ENST00000616242.5:c.*104A>T
|
ENSP00000482149.2:n.*104A>T
|
|
ENST00000683378.1:n.210A>T
|
|
|
ENST00000345378.7:c.987A>T
|
ENSP00000223366.2:p.Gly329=
|
|
ENST00000403799.8:c.984A>T
MANE Select
|
ENSP00000384247.3:p.Gly328=
|
|
ENST00000671824.1:c.1047A>T
|
ENSP00000500264.1:p.Gly349=
|
|
ENST00000673284.1:c.984A>T
|
ENSP00000499852.1:p.Gly328=
|
|
ENST00000345378.6:c.987A>T
|
ENSP00000223366.2:p.Gly329=
|
|
ENST00000395796.7:c.981A>T
|
ENSP00000379142.3:p.Gly327=
|
|
ENST00000403799.7:c.984A>T
|
ENSP00000384247.3:p.Gly328=
|
|
ENST00000437084.1:c.933A>T
|
ENSP00000402840.1:p.Gly311=
|
|
ENST00000473353.1:n.282A>T
|
|
|
ENST00000616242.4:c.981A>T
|
ENSP00000482149.1:p.Gly327=
|
|
NM_000162.3:c.984A>T
|
NP_000153.1:p.Gly328=
|
|
NM_033507.1:c.987A>T
|
NP_277042.1:p.Gly329=
|
|
NM_033508.1:c.981A>T
|
NP_277043.1:p.Gly327=
|
|
NM_000162.4:c.984A>T
|
NP_000153.1:p.Gly328=
|
|
NM_001354800.1:c.984A>T
|
NP_001341729.1:p.Gly328=
|
|
NM_001354801.1:c.8+121A>T
|
NP_001341730.1:n.8+121A>T
|
|
NM_033507.2:c.987A>T
|
NP_277042.1:p.Gly329=
|
|
NM_033508.2:c.981A>T
|
NP_277043.1:p.Gly327=
|
|
NM_000162.5:c.984A>T
MANE Select
|
NP_000153.1:p.Gly328=
|
|
NM_033507.3:c.987A>T
|
NP_277042.1:p.Gly329=
|
|
NM_033508.3:c.981A>T
|
NP_277043.1:p.Gly327=
|
|