ENST00000209873.9:c.1518T>G
MANE Select
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ENSP00000209873.4:p.Ala506=
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ENST00000546562.6:n.2582T>G
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|
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ENST00000547238.6:n.2154T>G
|
|
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ENST00000547520.6:n.1634T>G
|
|
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ENST00000547757.2:c.*436T>G
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ENSP00000448020.2:n.*436T>G
|
|
ENST00000548931.6:c.953T>G
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ENSP00000457518.1:p.Leu318Arg
|
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ENST00000549450.6:n.1452T>G
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|
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ENST00000672797.1:n.2007T>G
|
|
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ENST00000209873.8:c.1518T>G
|
ENSP00000209873.4:p.Ala506=
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|
ENST00000394384.7:c.1419T>G
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ENSP00000377908.3:p.Ala473=
|
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ENST00000548931.5:c.953T>G
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ENSP00000457518.1:p.Leu318Arg
|
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ENST00000550286.5:c.1146T>G
|
ENSP00000446885.1:p.Ala382=
|
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ENST00000552876.5:n.1861T>G
|
|
|
NM_001173466.1:c.1419T>G
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NP_001166937.1:p.Ala473=
|
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NM_015665.5:c.1518T>G
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NP_056480.1:p.Ala506=
|
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XM_006719617.2:c.1533T>G
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XP_006719680.1:p.Ala511=
|
|
XM_011538777.1:c.1575T>G
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XP_011537079.1:p.Ala525=
|
|
XM_011538778.1:c.1560T>G
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XP_011537080.1:p.Ala520=
|
|
XM_011538779.1:c.1476T>G
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XP_011537081.1:p.Ala492=
|
|
XM_011538780.1:c.1461T>G
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XP_011537082.1:p.Ala487=
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XM_011538781.1:c.909T>G
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XP_011537083.1:p.Ala303=
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XM_011538778.2:c.1560T>G
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XP_011537080.1:p.Ala520=
|
|
XM_011538780.2:c.1461T>G
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XP_011537082.1:p.Ala487=
|
|
XR_001748875.2:n.1575T>G
|
|
|
NM_015665.6:c.1518T>G
MANE Select
|
NP_056480.1:p.Ala506=
|
|
NM_001173466.2:c.1419T>G
|
NP_001166937.1:p.Ala473=
|
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