ENST00000209873.9:c.1431C>G
MANE Select
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ENSP00000209873.4:p.Gly477=
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ENST00000546562.6:n.2495C>G
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ENST00000547238.6:n.2067C>G
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ENST00000547520.6:n.1547C>G
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ENST00000547757.2:c.*349C>G
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ENSP00000448020.2:n.*349C>G
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ENST00000548880.2:n.1881C>G
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|
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ENST00000548931.6:c.866C>G
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ENSP00000457518.1:p.Ala289Gly
|
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ENST00000549450.6:n.1365C>G
|
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ENST00000552161.6:n.2509C>G
|
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ENST00000672797.1:n.1920C>G
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ENST00000209873.8:c.1431C>G
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ENSP00000209873.4:p.Gly477=
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ENST00000394384.7:c.1332C>G
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ENSP00000377908.3:p.Gly444=
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|
ENST00000548931.5:c.866C>G
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ENSP00000457518.1:p.Ala289Gly
|
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ENST00000550286.5:c.1059C>G
|
ENSP00000446885.1:p.Gly353=
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ENST00000552876.5:n.1774C>G
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|
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NM_001173466.1:c.1332C>G
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NP_001166937.1:p.Gly444=
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NM_015665.5:c.1431C>G
|
NP_056480.1:p.Gly477=
|
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XM_006719617.2:c.1446C>G
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XP_006719680.1:p.Gly482=
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XM_011538777.1:c.1488C>G
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XP_011537079.1:p.Gly496=
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XM_011538778.1:c.1473C>G
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XP_011537080.1:p.Gly491=
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XM_011538779.1:c.1389C>G
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XP_011537081.1:p.Gly463=
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XM_011538780.1:c.1374C>G
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XP_011537082.1:p.Gly458=
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XM_011538781.1:c.822C>G
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XP_011537083.1:p.Gly274=
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XM_011538778.2:c.1473C>G
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XP_011537080.1:p.Gly491=
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XM_011538780.2:c.1374C>G
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XP_011537082.1:p.Gly458=
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XR_001748875.2:n.1488C>G
|
|
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NM_015665.6:c.1431C>G
MANE Select
|
NP_056480.1:p.Gly477=
|
|
NM_001173466.2:c.1332C>G
|
NP_001166937.1:p.Gly444=
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