ENST00000636937.2:c.1074G>A
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ENSP00000516154.1:p.Glu358=
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|
ENST00000268124.11:c.1074G>A
MANE Select
|
ENSP00000268124.5:p.Glu358=
|
|
ENST00000530292.3:c.675G>A
|
ENSP00000432885.2:p.Glu225=
|
|
ENST00000635986.2:c.1074G>A
|
ENSP00000490653.2:p.Glu358=
|
|
ENST00000636774.1:c.1074G>A
|
ENSP00000489799.1:p.Glu358=
|
|
ENST00000637264.1:c.146G>A
|
|
|
ENST00000666746.1:c.731G>A
|
|
|
ENST00000672071.1:n.1272G>A
|
|
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ENST00000672923.2:n.71G>A
|
|
|
ENST00000268124.9:c.1074G>A
|
ENSP00000268124.5:p.Glu358=
|
|
ENST00000442287.6:c.1074G>A
|
ENSP00000399851.2:p.Glu358=
|
|
ENST00000631044.2:c.*457G>A
|
ENSP00000486730.1:n.*457G>A
|
|
NM_001126131.1:c.1074G>A
|
NP_001119603.1:p.Glu358=
|
|
NM_002693.2:c.1074G>A
|
NP_002684.1:p.Glu358=
|
|
NM_001126131.2:c.1074G>A
|
NP_001119603.1:p.Glu358=
|
|
NM_002693.3:c.1074G>A
MANE Select
|
NP_002684.1:p.Glu358=
|
|