ENST00000209873.9:c.1419C>G
MANE Select
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ENSP00000209873.4:p.Gly473=
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ENST00000546562.6:n.2483C>G
|
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ENST00000547238.6:n.2055C>G
|
|
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ENST00000547520.6:n.1535C>G
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|
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ENST00000547757.2:c.*337C>G
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ENSP00000448020.2:n.*337C>G
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ENST00000548880.2:n.1869C>G
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|
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ENST00000548931.6:c.854C>G
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ENSP00000457518.1:p.Ala285Gly
|
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ENST00000549450.6:n.1353C>G
|
|
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ENST00000552161.6:n.2497C>G
|
|
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ENST00000672797.1:n.1908C>G
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ENST00000209873.8:c.1419C>G
|
ENSP00000209873.4:p.Gly473=
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|
ENST00000394384.7:c.1320C>G
|
ENSP00000377908.3:p.Gly440=
|
|
ENST00000548931.5:c.854C>G
|
ENSP00000457518.1:p.Ala285Gly
|
|
ENST00000550286.5:c.1047C>G
|
ENSP00000446885.1:p.Gly349=
|
|
ENST00000552876.5:n.1762C>G
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|
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NM_001173466.1:c.1320C>G
|
NP_001166937.1:p.Gly440=
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|
NM_015665.5:c.1419C>G
|
NP_056480.1:p.Gly473=
|
|
XM_006719617.2:c.1434C>G
|
XP_006719680.1:p.Gly478=
|
|
XM_011538777.1:c.1476C>G
|
XP_011537079.1:p.Gly492=
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XM_011538778.1:c.1461C>G
|
XP_011537080.1:p.Gly487=
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XM_011538779.1:c.1377C>G
|
XP_011537081.1:p.Gly459=
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|
XM_011538780.1:c.1362C>G
|
XP_011537082.1:p.Gly454=
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XM_011538781.1:c.810C>G
|
XP_011537083.1:p.Gly270=
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XM_011538778.2:c.1461C>G
|
XP_011537080.1:p.Gly487=
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|
XM_011538780.2:c.1362C>G
|
XP_011537082.1:p.Gly454=
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XR_001748875.2:n.1476C>G
|
|
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NM_015665.6:c.1419C>G
MANE Select
|
NP_056480.1:p.Gly473=
|
|
NM_001173466.2:c.1320C>G
|
NP_001166937.1:p.Gly440=
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