ENST00000338034.9:c.2329G>C
MANE Select
|
ENSP00000337445.4:p.Glu777Gln
|
|
ENST00000338034.8:c.2329G>C
|
ENSP00000337445.4:p.Glu777Gln
|
|
ENST00000395962.6:c.2272G>C
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ENSP00000379291.1:p.Glu758Gln
|
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ENST00000426905.7:c.2209G>C
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ENSP00000405223.3:p.Glu737Gln
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ENST00000465825.5:n.2216G>C
|
|
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ENST00000480891.5:n.2158G>C
|
|
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ENST00000484122.5:n.3159G>C
|
|
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ENST00000487229.6:n.1875G>C
|
|
|
ENST00000584650.5:c.1728G>C
|
|
|
NM_001165962.1:c.2209G>C
|
NP_001159434.1:p.Glu737Gln
|
|
NM_018127.6:c.2329G>C
|
NP_060597.4:p.Glu777Gln
|
|
NM_173717.1:c.2326G>C
|
NP_776065.1:p.Glu776Gln
|
|
XM_024450850.1:c.2488G>C
|
XP_024306618.1:p.Glu830Gln
|
|
XM_024450851.1:c.2410G>C
|
XP_024306619.1:p.Glu804Gln
|
|
XM_024450852.1:c.2407G>C
|
XP_024306620.1:p.Glu803Gln
|
|
XM_024450853.1:c.2404G>C
|
XP_024306621.1:p.Glu802Gln
|
|
XM_024450854.1:c.2368G>C
|
XP_024306622.1:p.Glu790Gln
|
|
XM_024450855.1:c.2287G>C
|
XP_024306623.1:p.Glu763Gln
|
|
XM_024450856.1:c.2206G>C
|
XP_024306624.1:p.Glu736Gln
|
|
XM_024450857.1:c.2206G>C
|
XP_024306625.1:p.Glu736Gln
|
|
XM_024450858.1:c.2125G>C
|
XP_024306626.1:p.Glu709Gln
|
|
XM_024450859.1:c.2122G>C
|
XP_024306627.1:p.Glu708Gln
|
|
XM_024450860.1:c.2047G>C
|
XP_024306628.1:p.Glu683Gln
|
|
XM_024450861.1:c.2047G>C
|
XP_024306629.1:p.Glu683Gln
|
|
XM_024450862.1:c.2044G>C
|
XP_024306630.1:p.Glu682Gln
|
|
NM_018127.7:c.2329G>C
MANE Select
|
NP_060597.4:p.Glu777Gln
|
|
NM_001165962.2:c.2209G>C
|
NP_001159434.1:p.Glu737Gln
|
|
NM_173717.2:c.2326G>C
|
NP_776065.1:p.Glu776Gln
|
|