ENST00000209873.9:c.1001G>A
MANE Select
|
ENSP00000209873.4:p.Gly334Asp
|
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ENST00000546393.7:n.1846G>A
|
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ENST00000546562.6:n.2065G>A
|
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ENST00000547238.6:n.1637G>A
|
|
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ENST00000547520.6:n.995G>A
|
|
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ENST00000547757.2:c.50G>A
|
ENSP00000448020.2:p.Gly17Asp
|
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ENST00000548880.2:n.1451G>A
|
|
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ENST00000548931.6:c.521G>A
|
ENSP00000457518.1:p.Gly174Asp
|
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ENST00000549450.6:n.935G>A
|
|
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ENST00000552161.6:n.1957G>A
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ENST00000672797.1:n.1490G>A
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|
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ENST00000672900.1:n.1943G>A
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|
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ENST00000209873.8:c.1001G>A
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ENSP00000209873.4:p.Gly334Asp
|
|
ENST00000394384.7:c.902G>A
|
ENSP00000377908.3:p.Gly301Asp
|
|
ENST00000547520.5:n.705G>A
|
|
|
ENST00000548931.5:c.521G>A
|
ENSP00000457518.1:p.Gly174Asp
|
|
ENST00000550033.5:n.256G>A
|
|
|
ENST00000550286.5:c.629G>A
|
ENSP00000446885.1:p.Gly210Asp
|
|
ENST00000552876.5:n.1344G>A
|
|
|
NM_001173466.1:c.902G>A
|
NP_001166937.1:p.Gly301Asp
|
|
NM_015665.5:c.1001G>A
|
NP_056480.1:p.Gly334Asp
|
|
XM_006719617.2:c.1016G>A
|
XP_006719680.1:p.Gly339Asp
|
|
XM_006719619.2:c.*11G>A
|
XP_006719682.1:n.*11G>A
|
|
XM_011538777.1:c.1016G>A
|
XP_011537079.1:p.Gly339Asp
|
|
XM_011538778.1:c.1001G>A
|
XP_011537080.1:p.Gly334Asp
|
|
XM_011538779.1:c.917G>A
|
XP_011537081.1:p.Gly306Asp
|
|
XM_011538780.1:c.902G>A
|
XP_011537082.1:p.Gly301Asp
|
|
XM_011538781.1:c.350G>A
|
XP_011537083.1:p.Gly117Asp
|
|
XM_011538778.2:c.1001G>A
|
XP_011537080.1:p.Gly334Asp
|
|
XM_011538780.2:c.902G>A
|
XP_011537082.1:p.Gly301Asp
|
|
XR_001748875.2:n.1058G>A
|
|
|
NM_015665.6:c.1001G>A
MANE Select
|
NP_056480.1:p.Gly334Asp
|
|
NM_001173466.2:c.902G>A
|
NP_001166937.1:p.Gly301Asp
|
|