ENST00000376649.8:c.660G>C
MANE Select
|
ENSP00000365837.3:p.Glu220Asp
|
|
ENST00000322060.9:c.576G>C
|
ENSP00000324726.5:p.Glu192Asp
|
|
ENST00000376649.7:c.660G>C
|
ENSP00000365837.3:p.Glu220Asp
|
|
ENST00000443358.6:c.576G>C
|
ENSP00000392451.2:p.Glu192Asp
|
|
ENST00000535067.5:c.358-2132G>C
|
ENSP00000443969.1:n.358-2132G>C
|
|
ENST00000537484.1:c.585G>C
|
ENSP00000440179.1:p.Glu195Asp
|
|
ENST00000542167.2:c.501G>C
|
ENSP00000438948.1:p.Glu167Asp
|
|
ENST00000543754.1:n.481G>C
|
|
|
NM_001002019.2:c.576G>C
|
NP_001002019.1:p.Glu192Asp
|
|
NM_001002020.2:c.576G>C
|
NP_001002020.1:p.Glu192Asp
|
|
NM_025215.5:c.660G>C
|
NP_079491.2:p.Glu220Asp
|
|
XM_011538768.1:c.261G>C
|
XP_011537070.1:p.Glu87Asp
|
|
XM_011538768.3:c.261G>C
|
XP_011537070.1:p.Glu87Asp
|
|
XR_001748872.1:n.1115G>C
|
|
|
NM_001002019.3:c.576G>C
|
NP_001002019.1:p.Glu192Asp
|
|
NM_001002020.3:c.576G>C
|
NP_001002020.1:p.Glu192Asp
|
|
NM_025215.6:c.660G>C
MANE Select
|
NP_079491.2:p.Glu220Asp
|
|