ENST00000209873.9:c.1531T>G
MANE Select
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ENSP00000209873.4:p.Ser511Ala
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ENST00000546562.6:n.2595T>G
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ENST00000547238.6:n.2167T>G
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ENST00000547520.6:n.1647T>G
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ENST00000547757.2:c.*449T>G
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ENSP00000448020.2:n.*449T>G
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ENST00000548931.6:c.966T>G
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ENSP00000457518.1:p.Ala322=
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ENST00000549450.6:n.1465T>G
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ENST00000672797.1:n.2020T>G
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ENST00000209873.8:c.1531T>G
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ENSP00000209873.4:p.Ser511Ala
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ENST00000394384.7:c.1432T>G
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ENSP00000377908.3:p.Ser478Ala
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ENST00000548931.5:c.966T>G
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ENSP00000457518.1:p.Ala322=
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ENST00000550286.5:c.1159T>G
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ENSP00000446885.1:p.Ser387Ala
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ENST00000552876.5:n.1874T>G
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|
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NM_001173466.1:c.1432T>G
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NP_001166937.1:p.Ser478Ala
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NM_015665.5:c.1531T>G
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NP_056480.1:p.Ser511Ala
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XM_006719617.2:c.1546T>G
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XP_006719680.1:p.Ser516Ala
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XM_011538777.1:c.1588T>G
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XP_011537079.1:p.Ser530Ala
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XM_011538778.1:c.1573T>G
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XP_011537080.1:p.Ser525Ala
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XM_011538779.1:c.1489T>G
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XP_011537081.1:p.Ser497Ala
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XM_011538780.1:c.1474T>G
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XP_011537082.1:p.Ser492Ala
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XM_011538781.1:c.922T>G
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XP_011537083.1:p.Ser308Ala
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XM_011538778.2:c.1573T>G
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XP_011537080.1:p.Ser525Ala
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XM_011538780.2:c.1474T>G
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XP_011537082.1:p.Ser492Ala
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XR_001748875.2:n.1588T>G
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NM_015665.6:c.1531T>G
MANE Select
|
NP_056480.1:p.Ser511Ala
|
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NM_001173466.2:c.1432T>G
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NP_001166937.1:p.Ser478Ala
|
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