ENST00000537228.6:c.427+77G=
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ENSP00000445691.1:n.427+77G=
|
|
ENST00000543081.6:c.427+77G=
|
ENSP00000439103.2:n.427+77G=
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ENST00000544516.6:c.157-801G=
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ENSP00000439538.2:n.157-801G=
|
|
ENST00000545576.2:n.613G=
|
|
|
ENST00000696246.1:c.412+77G=
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ENSP00000512504.1:n.412+77G=
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|
ENST00000696271.1:n.624G=
|
|
|
ENST00000696272.1:c.412+77G=
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ENSP00000512515.1:n.412+77G=
|
|
ENST00000696273.1:c.460+77G=
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ENSP00000512516.1:n.460+77G=
|
|
ENST00000229335.11:c.427+77G=
MANE Select
|
ENSP00000229335.6:n.427+77G=
|
|
ENST00000229335.10:c.427+77G=
|
ENSP00000229335.6:n.427+77G=
|
|
ENST00000537228.5:c.427+77G=
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ENSP00000445691.1:n.427+77G=
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|
ENST00000543081.5:c.423+77G=
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|
|
ENST00000544516.5:c.153-801G=
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|
|
ENST00000545512.1:c.423+77G=
|
|
|
ENST00000545576.1:n.538G=
|
|
|
NM_020661.2:c.427+77G= , LRG_17t1:c.427+77G=
|
NP_065712.1:n.427+77G=
|
|
XM_011520772.1:c.427+77G=
|
XP_011519074.1:n.427+77G=
|
|
XM_011520773.1:c.427+77G=
|
XP_011519075.1:n.427+77G=
|
|
NM_001330343.1:c.427+77G=
|
NP_001317272.1:n.427+77G=
|
|
NM_020661.3:c.427+77G=
|
NP_065712.1:n.427+77G=
|
|
XM_011520773.2:c.427+77G=
|
XP_011519075.1:n.427+77G=
|
|
NM_020661.4:c.427+77G=
MANE Select
|
NP_065712.1:n.427+77G=
|
|
NM_001330343.2:c.427+77G=
|
NP_001317272.1:n.427+77G=
|
|