ENST00000209873.9:c.1526G>A
MANE Select
|
ENSP00000209873.4:p.Gly509Glu
|
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ENST00000546562.6:n.2590G>A
|
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ENST00000547238.6:n.2162G>A
|
|
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ENST00000547520.6:n.1642G>A
|
|
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ENST00000547757.2:c.*444G>A
|
ENSP00000448020.2:n.*444G>A
|
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ENST00000548931.6:c.961G>A
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ENSP00000457518.1:p.Glu321Lys
|
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ENST00000549450.6:n.1460G>A
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|
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ENST00000672797.1:n.2015G>A
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|
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ENST00000209873.8:c.1526G>A
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ENSP00000209873.4:p.Gly509Glu
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ENST00000394384.7:c.1427G>A
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ENSP00000377908.3:p.Gly476Glu
|
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ENST00000548931.5:c.961G>A
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ENSP00000457518.1:p.Glu321Lys
|
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ENST00000550286.5:c.1154G>A
|
ENSP00000446885.1:p.Gly385Glu
|
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ENST00000552876.5:n.1869G>A
|
|
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NM_001173466.1:c.1427G>A
|
NP_001166937.1:p.Gly476Glu
|
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NM_015665.5:c.1526G>A
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NP_056480.1:p.Gly509Glu
|
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XM_006719617.2:c.1541G>A
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XP_006719680.1:p.Gly514Glu
|
|
XM_011538777.1:c.1583G>A
|
XP_011537079.1:p.Gly528Glu
|
|
XM_011538778.1:c.1568G>A
|
XP_011537080.1:p.Gly523Glu
|
|
XM_011538779.1:c.1484G>A
|
XP_011537081.1:p.Gly495Glu
|
|
XM_011538780.1:c.1469G>A
|
XP_011537082.1:p.Gly490Glu
|
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XM_011538781.1:c.917G>A
|
XP_011537083.1:p.Gly306Glu
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XM_011538778.2:c.1568G>A
|
XP_011537080.1:p.Gly523Glu
|
|
XM_011538780.2:c.1469G>A
|
XP_011537082.1:p.Gly490Glu
|
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XR_001748875.2:n.1583G>A
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|
|
NM_015665.6:c.1526G>A
MANE Select
|
NP_056480.1:p.Gly509Glu
|
|
NM_001173466.2:c.1427G>A
|
NP_001166937.1:p.Gly476Glu
|
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