ENST00000209873.9:c.1467C>G
MANE Select
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ENSP00000209873.4:p.Ala489=
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ENST00000546562.6:n.2531C>G
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|
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ENST00000547238.6:n.2103C>G
|
|
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ENST00000547520.6:n.1583C>G
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|
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ENST00000547757.2:c.*385C>G
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ENSP00000448020.2:n.*385C>G
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ENST00000548880.2:n.1917C>G
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|
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ENST00000548931.6:c.902C>G
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ENSP00000457518.1:p.Pro301Arg
|
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ENST00000549450.6:n.1401C>G
|
|
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ENST00000552161.6:n.2545C>G
|
|
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ENST00000672797.1:n.1956C>G
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|
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ENST00000209873.8:c.1467C>G
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ENSP00000209873.4:p.Ala489=
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|
ENST00000394384.7:c.1368C>G
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ENSP00000377908.3:p.Ala456=
|
|
ENST00000548931.5:c.902C>G
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ENSP00000457518.1:p.Pro301Arg
|
|
ENST00000550286.5:c.1095C>G
|
ENSP00000446885.1:p.Ala365=
|
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ENST00000552876.5:n.1810C>G
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|
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NM_001173466.1:c.1368C>G
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NP_001166937.1:p.Ala456=
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|
NM_015665.5:c.1467C>G
|
NP_056480.1:p.Ala489=
|
|
XM_006719617.2:c.1482C>G
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XP_006719680.1:p.Ala494=
|
|
XM_011538777.1:c.1524C>G
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XP_011537079.1:p.Ala508=
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|
XM_011538778.1:c.1509C>G
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XP_011537080.1:p.Ala503=
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|
XM_011538779.1:c.1425C>G
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XP_011537081.1:p.Ala475=
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|
XM_011538780.1:c.1410C>G
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XP_011537082.1:p.Ala470=
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XM_011538781.1:c.858C>G
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XP_011537083.1:p.Ala286=
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XM_011538778.2:c.1509C>G
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XP_011537080.1:p.Ala503=
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|
XM_011538780.2:c.1410C>G
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XP_011537082.1:p.Ala470=
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XR_001748875.2:n.1524C>G
|
|
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NM_015665.6:c.1467C>G
MANE Select
|
NP_056480.1:p.Ala489=
|
|
NM_001173466.2:c.1368C>G
|
NP_001166937.1:p.Ala456=
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