ENST00000261819.8:c.1695A>G
MANE Select
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ENSP00000261819.3:p.Gln565=
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ENST00000261819.7:c.1695A>G
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ENSP00000261819.3:p.Gln565=
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|
ENST00000366333.3:n.907A>G
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|
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ENST00000441917.6:c.1359A>G
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ENSP00000415061.2:p.Gln453=
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ENST00000534976.5:n.2351A>G
|
|
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ENST00000535482.1:c.693A>G
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ENSP00000438754.1:p.Gln231=
|
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ENST00000535641.5:n.1906A>G
|
|
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ENST00000539079.5:c.1039A>G
|
|
|
ENST00000541887.5:c.1656A>G
|
ENSP00000439875.1:p.Gln552=
|
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ENST00000544314.5:n.813A>G
|
|
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ENST00000545218.5:n.938A>G
|
|
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NM_001137559.1:c.1359A>G
|
NP_001131031.1:p.Gln453=
|
|
NM_016237.4:c.1695A>G
|
NP_057321.2:p.Gln565=
|
|
XM_005253900.2:c.1656A>G
|
XP_005253957.1:p.Gln552=
|
|
XM_006719449.1:c.501A>G
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XP_006719512.1:p.Gln167=
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|
NM_001330489.1:c.1656A>G
|
NP_001317418.1:p.Gln552=
|
|
XM_017019423.2:c.501A>G
|
XP_016874912.1:p.Gln167=
|
|
XM_017019424.2:c.501A>G
|
XP_016874913.1:p.Gln167=
|
|
NM_016237.5:c.1695A>G
MANE Select
|
NP_057321.2:p.Gln565=
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|
NM_001330489.2:c.1656A>G
|
NP_001317418.1:p.Gln552=
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