ENST00000209873.9:c.1432C>G
MANE Select
|
ENSP00000209873.4:p.Arg478Gly
|
|
ENST00000546562.6:n.2496C>G
|
|
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ENST00000547238.6:n.2068C>G
|
|
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ENST00000547520.6:n.1548C>G
|
|
|
ENST00000547757.2:c.*350C>G
|
ENSP00000448020.2:n.*350C>G
|
|
ENST00000548880.2:n.1882C>G
|
|
|
ENST00000548931.6:c.867C>G
|
ENSP00000457518.1:p.Ala289=
|
|
ENST00000549450.6:n.1366C>G
|
|
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ENST00000552161.6:n.2510C>G
|
|
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ENST00000672797.1:n.1921C>G
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|
|
ENST00000209873.8:c.1432C>G
|
ENSP00000209873.4:p.Arg478Gly
|
|
ENST00000394384.7:c.1333C>G
|
ENSP00000377908.3:p.Arg445Gly
|
|
ENST00000548931.5:c.867C>G
|
ENSP00000457518.1:p.Ala289=
|
|
ENST00000550286.5:c.1060C>G
|
ENSP00000446885.1:p.Arg354Gly
|
|
ENST00000552876.5:n.1775C>G
|
|
|
NM_001173466.1:c.1333C>G
|
NP_001166937.1:p.Arg445Gly
|
|
NM_015665.5:c.1432C>G
|
NP_056480.1:p.Arg478Gly
|
|
XM_006719617.2:c.1447C>G
|
XP_006719680.1:p.Arg483Gly
|
|
XM_011538777.1:c.1489C>G
|
XP_011537079.1:p.Arg497Gly
|
|
XM_011538778.1:c.1474C>G
|
XP_011537080.1:p.Arg492Gly
|
|
XM_011538779.1:c.1390C>G
|
XP_011537081.1:p.Arg464Gly
|
|
XM_011538780.1:c.1375C>G
|
XP_011537082.1:p.Arg459Gly
|
|
XM_011538781.1:c.823C>G
|
XP_011537083.1:p.Arg275Gly
|
|
XM_011538778.2:c.1474C>G
|
XP_011537080.1:p.Arg492Gly
|
|
XM_011538780.2:c.1375C>G
|
XP_011537082.1:p.Arg459Gly
|
|
XR_001748875.2:n.1489C>G
|
|
|
NM_015665.6:c.1432C>G
MANE Select
|
NP_056480.1:p.Arg478Gly
|
|
NM_001173466.2:c.1333C>G
|
NP_001166937.1:p.Arg445Gly
|
|