ENST00000682568.1:n.1853A>G
|
|
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ENST00000682617.1:c.1913A>G
|
ENSP00000507912.1:p.Glu638Gly
|
|
ENST00000682826.1:c.*1089A>G
|
ENSP00000507274.1:n.*1089A>G
|
|
ENST00000682909.1:n.3815A>G
|
|
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ENST00000683277.1:n.3420A>G
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ENST00000683407.1:n.1783A>G
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|
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ENST00000683962.1:c.*1469A>G
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ENSP00000506854.1:n.*1469A>G
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ENST00000311895.8:c.1775A>G
MANE Select
|
ENSP00000310520.7:p.Glu592Gly
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ENST00000311895.7:c.1775A>G
|
ENSP00000310520.7:p.Glu592Gly
|
|
ENST00000389138.7:n.1052A>G
|
|
|
NM_005236.2:c.1775A>G , LRG_463t1:c.1775A>G
|
NP_005227.1:p.Glu592Gly
|
|
XM_011522424.1:c.1913A>G
|
XP_011520726.1:p.Glu638Gly
|
|
XM_011522425.1:c.1232A>G
|
XP_011520727.1:p.Glu411Gly
|
|
XM_011522426.1:c.986A>G
|
XP_011520728.1:p.Glu329Gly
|
|
XM_011522427.1:c.425A>G
|
XP_011520729.1:p.Glu142Gly
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|
XR_932805.1:n.1934A>G
|
|
|
XM_011522424.3:c.1913A>G
|
XP_011520726.1:p.Glu638Gly
|
|
XM_017023043.2:c.986A>G
|
XP_016878532.1:p.Glu329Gly
|
|
NM_005236.3:c.1775A>G
MANE Select
|
NP_005227.1:p.Glu592Gly
|
|