ENST00000537228.6:c.471A>G
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ENSP00000445691.1:p.Glu157=
|
|
ENST00000543081.6:c.427+366A>G
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ENSP00000439103.2:n.427+366A>G
|
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ENST00000544516.6:c.157-512A>G
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ENSP00000439538.2:n.157-512A>G
|
|
ENST00000545576.2:n.902A>G
|
|
|
ENST00000696246.1:c.456A>G
|
ENSP00000512504.1:p.Glu152=
|
|
ENST00000696271.1:n.913A>G
|
|
|
ENST00000696272.1:c.486A>G
|
ENSP00000512515.1:p.Glu162=
|
|
ENST00000696273.1:c.534A>G
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ENSP00000512516.1:p.Glu178=
|
|
ENST00000229335.11:c.501A>G
MANE Select
|
ENSP00000229335.6:p.Glu167=
|
|
ENST00000229335.10:c.501A>G
|
ENSP00000229335.6:p.Glu167=
|
|
ENST00000537228.5:c.471A>G
|
ENSP00000445691.1:p.Glu157=
|
|
ENST00000543081.5:c.423+366A>G
|
|
|
ENST00000544516.5:c.153-512A>G
|
|
|
ENST00000545512.1:c.497A>G
|
|
|
ENST00000545576.1:n.827A>G
|
|
|
NM_020661.2:c.501A>G , LRG_17t1:c.501A>G
|
NP_065712.1:p.Glu167=
|
|
XM_011520772.1:c.471A>G
|
XP_011519074.1:p.Glu157=
|
|
XM_011520773.1:c.427+366A>G
|
XP_011519075.1:n.427+366A>G
|
|
NM_001330343.1:c.471A>G
|
NP_001317272.1:p.Glu157=
|
|
NM_020661.3:c.501A>G
|
NP_065712.1:p.Glu167=
|
|
XM_011520773.2:c.427+366A>G
|
XP_011519075.1:n.427+366A>G
|
|
NM_020661.4:c.501A>G
MANE Select
|
NP_065712.1:p.Glu167=
|
|
NM_001330343.2:c.471A>G
|
NP_001317272.1:p.Glu157=
|
|