ENST00000362012.7:c.576C>T
MANE Select
|
ENSP00000354612.2:p.Gly192=
|
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ENST00000373698.7:c.249C>T
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ENSP00000362802.5:p.Gly83=
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|
ENST00000426608.6:c.313-46C>T
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ENSP00000411606.2:n.313-46C>T
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ENST00000540753.6:c.501C>T
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ENSP00000437709.1:p.Gly167=
|
|
ENST00000619306.5:c.432C>T
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ENSP00000483540.2:p.Gly144=
|
|
ENST00000643576.1:n.670C>T
|
|
|
ENST00000643810.1:c.249C>T
|
ENSP00000494717.1:p.Gly83=
|
|
ENST00000645132.1:n.519+2877C>T
|
|
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ENST00000647067.1:c.*421C>T
|
ENSP00000495728.1:n.*421C>T
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|
ENST00000223423.8:c.576C>T
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ENSP00000223423.4:p.Gly192=
|
|
ENST00000362012.6:c.576C>T
|
ENSP00000354612.2:p.Gly192=
|
|
ENST00000373698.6:c.249C>T
|
ENSP00000362802.5:p.Gly83=
|
|
ENST00000426608.5:c.304-46C>T
|
ENSP00000411606.1:n.304-46C>T
|
|
ENST00000540753.5:c.501C>T
|
ENSP00000437709.1:p.Gly167=
|
|
ENST00000614910.4:c.432C>T
|
ENSP00000484800.1:p.Gly144=
|
|
ENST00000619306.4:c.669C>T
|
ENSP00000483540.1:p.Gly223=
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|
NM_000962.3:c.576C>T
|
NP_000953.2:p.Gly192=
|
|
NM_001271164.1:c.432C>T
|
NP_001258093.1:p.Gly144=
|
|
NM_001271165.1:c.249C>T
|
NP_001258094.1:p.Gly83=
|
|
NM_001271166.1:c.249C>T
|
NP_001258095.1:p.Gly83=
|
|
NM_001271367.1:c.249C>T
|
NP_001258296.1:p.Gly83=
|
|
NM_001271368.1:c.501C>T
|
NP_001258297.1:p.Gly167=
|
|
NM_080591.2:c.576C>T
|
NP_542158.1:p.Gly192=
|
|
XM_005252105.2:c.501C>T
|
XP_005252162.1:p.Gly167=
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|
XM_011518875.1:c.501C>T
|
XP_011517177.1:p.Gly167=
|
|
XM_011518876.1:c.249C>T
|
XP_011517178.1:p.Gly83=
|
|
XM_005252105.3:c.501C>T
|
XP_005252162.1:p.Gly167=
|
|
XM_011518875.2:c.501C>T
|
XP_011517177.1:p.Gly167=
|
|
XM_011518876.2:c.249C>T
|
XP_011517178.1:p.Gly83=
|
|
XM_024447614.1:c.249C>T
|
XP_024303382.1:p.Gly83=
|
|
XM_024447615.1:c.249C>T
|
XP_024303383.1:p.Gly83=
|
|
NM_000962.4:c.576C>T
MANE Select
|
NP_000953.2:p.Gly192=
|
|
NM_001271164.2:c.432C>T
|
NP_001258093.1:p.Gly144=
|
|
NM_001271165.2:c.249C>T
|
NP_001258094.1:p.Gly83=
|
|
NM_001271166.2:c.249C>T
|
NP_001258095.1:p.Gly83=
|
|
NM_001271367.2:c.249C>T
|
NP_001258296.1:p.Gly83=
|
|
NM_001271368.2:c.501C>T
|
NP_001258297.1:p.Gly167=
|
|
NM_080591.3:c.576C>T
|
NP_542158.1:p.Gly192=
|
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