ENST00000209873.9:c.1460T>G
MANE Select
|
ENSP00000209873.4:p.Val487Gly
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ENST00000546562.6:n.2524T>G
|
|
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ENST00000547238.6:n.2096T>G
|
|
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ENST00000547520.6:n.1576T>G
|
|
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ENST00000547757.2:c.*378T>G
|
ENSP00000448020.2:n.*378T>G
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ENST00000548880.2:n.1910T>G
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|
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ENST00000548931.6:c.895T>G
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ENSP00000457518.1:p.Ser299Ala
|
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ENST00000549450.6:n.1394T>G
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|
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ENST00000552161.6:n.2538T>G
|
|
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ENST00000672797.1:n.1949T>G
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ENST00000209873.8:c.1460T>G
|
ENSP00000209873.4:p.Val487Gly
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|
ENST00000394384.7:c.1361T>G
|
ENSP00000377908.3:p.Val454Gly
|
|
ENST00000548931.5:c.895T>G
|
ENSP00000457518.1:p.Ser299Ala
|
|
ENST00000550286.5:c.1088T>G
|
ENSP00000446885.1:p.Val363Gly
|
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ENST00000552876.5:n.1803T>G
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|
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NM_001173466.1:c.1361T>G
|
NP_001166937.1:p.Val454Gly
|
|
NM_015665.5:c.1460T>G
|
NP_056480.1:p.Val487Gly
|
|
XM_006719617.2:c.1475T>G
|
XP_006719680.1:p.Val492Gly
|
|
XM_011538777.1:c.1517T>G
|
XP_011537079.1:p.Val506Gly
|
|
XM_011538778.1:c.1502T>G
|
XP_011537080.1:p.Val501Gly
|
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XM_011538779.1:c.1418T>G
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XP_011537081.1:p.Val473Gly
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|
XM_011538780.1:c.1403T>G
|
XP_011537082.1:p.Val468Gly
|
|
XM_011538781.1:c.851T>G
|
XP_011537083.1:p.Val284Gly
|
|
XM_011538778.2:c.1502T>G
|
XP_011537080.1:p.Val501Gly
|
|
XM_011538780.2:c.1403T>G
|
XP_011537082.1:p.Val468Gly
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XR_001748875.2:n.1517T>G
|
|
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NM_015665.6:c.1460T>G
MANE Select
|
NP_056480.1:p.Val487Gly
|
|
NM_001173466.2:c.1361T>G
|
NP_001166937.1:p.Val454Gly
|
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