ENST00000682568.1:n.1823A>G
|
|
|
ENST00000682617.1:c.1883A>G
|
ENSP00000507912.1:p.Asp628Gly
|
|
ENST00000682826.1:c.*1059A>G
|
ENSP00000507274.1:n.*1059A>G
|
|
ENST00000682909.1:n.3785A>G
|
|
|
ENST00000683277.1:n.3390A>G
|
|
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ENST00000683407.1:n.1753A>G
|
|
|
ENST00000683962.1:c.*1439A>G
|
ENSP00000506854.1:n.*1439A>G
|
|
ENST00000311895.8:c.1745A>G
MANE Select
|
ENSP00000310520.7:p.Asp582Gly
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|
ENST00000311895.7:c.1745A>G
|
ENSP00000310520.7:p.Asp582Gly
|
|
ENST00000389138.7:n.1022A>G
|
|
|
NM_005236.2:c.1745A>G , LRG_463t1:c.1745A>G
|
NP_005227.1:p.Asp582Gly
|
|
XM_011522424.1:c.1883A>G
|
XP_011520726.1:p.Asp628Gly
|
|
XM_011522425.1:c.1202A>G
|
XP_011520727.1:p.Asp401Gly
|
|
XM_011522426.1:c.956A>G
|
XP_011520728.1:p.Asp319Gly
|
|
XM_011522427.1:c.395A>G
|
XP_011520729.1:p.Asp132Gly
|
|
XR_932805.1:n.1904A>G
|
|
|
XM_011522424.3:c.1883A>G
|
XP_011520726.1:p.Asp628Gly
|
|
XM_017023043.2:c.956A>G
|
XP_016878532.1:p.Asp319Gly
|
|
NM_005236.3:c.1745A>G
MANE Select
|
NP_005227.1:p.Asp582Gly
|
|