ENST00000636937.2:c.1482A>G
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ENSP00000516154.1:p.Glu494=
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ENST00000268124.11:c.1482A>G
MANE Select
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ENSP00000268124.5:p.Glu494=
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ENST00000530292.3:c.1083A>G
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ENSP00000432885.2:p.Glu361=
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|
ENST00000635986.2:c.1482A>G
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ENSP00000490653.2:p.Glu494=
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ENST00000636774.1:c.*49A>G
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ENSP00000489799.1:n.*49A>G
|
|
ENST00000637238.1:c.219A>G
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ENSP00000490756.1:p.Glu73=
|
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ENST00000637264.1:c.554A>G
|
|
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ENST00000666746.1:c.1059A>G
|
|
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ENST00000672071.1:n.1680A>G
|
|
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ENST00000672923.2:n.1585A>G
|
|
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ENST00000268124.9:c.1482A>G
|
ENSP00000268124.5:p.Glu494=
|
|
ENST00000442287.6:c.1482A>G
|
ENSP00000399851.2:p.Glu494=
|
|
ENST00000532363.2:n.443A>G
|
|
|
ENST00000631044.2:c.*865A>G
|
ENSP00000486730.1:n.*865A>G
|
|
NM_001126131.1:c.1482A>G
|
NP_001119603.1:p.Glu494=
|
|
NM_002693.2:c.1482A>G
|
NP_002684.1:p.Glu494=
|
|
NM_001126131.2:c.1482A>G
|
NP_001119603.1:p.Glu494=
|
|
NM_002693.3:c.1482A>G
MANE Select
|
NP_002684.1:p.Glu494=
|
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