ENST00000682568.1:n.1800G>A
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|
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ENST00000682617.1:c.1860G>A
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ENSP00000507912.1:p.Glu620=
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ENST00000682826.1:c.*1036G>A
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ENSP00000507274.1:n.*1036G>A
|
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ENST00000682909.1:n.3762G>A
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|
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ENST00000683277.1:n.3367G>A
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|
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ENST00000683407.1:n.1730G>A
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|
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ENST00000683962.1:c.*1416G>A
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ENSP00000506854.1:n.*1416G>A
|
|
ENST00000311895.8:c.1722G>A
MANE Select
|
ENSP00000310520.7:p.Glu574=
|
|
ENST00000311895.7:c.1722G>A
|
ENSP00000310520.7:p.Glu574=
|
|
ENST00000389138.7:n.999G>A
|
|
|
NM_005236.2:c.1722G>A , LRG_463t1:c.1722G>A
|
NP_005227.1:p.Glu574=
|
|
XM_011522424.1:c.1860G>A
|
XP_011520726.1:p.Glu620=
|
|
XM_011522425.1:c.1179G>A
|
XP_011520727.1:p.Glu393=
|
|
XM_011522426.1:c.933G>A
|
XP_011520728.1:p.Glu311=
|
|
XM_011522427.1:c.372G>A
|
XP_011520729.1:p.Glu124=
|
|
XR_932805.1:n.1881G>A
|
|
|
XM_011522424.3:c.1860G>A
|
XP_011520726.1:p.Glu620=
|
|
XM_017023043.2:c.933G>A
|
XP_016878532.1:p.Glu311=
|
|
NM_005236.3:c.1722G>A
MANE Select
|
NP_005227.1:p.Glu574=
|
|