ENST00000682617.1:c.2740C>G
|
ENSP00000507912.1:p.His914Asp
|
|
ENST00000683962.1:c.*2296C>G
|
ENSP00000506854.1:n.*2296C>G
|
|
ENST00000311895.8:c.2602C>G
MANE Select
|
ENSP00000310520.7:p.His868Asp
|
|
ENST00000311895.7:c.2602C>G
|
ENSP00000310520.7:p.His868Asp
|
|
ENST00000389138.7:n.1879C>G
|
|
|
NM_005236.2:c.2602C>G , LRG_463t1:c.2602C>G
|
NP_005227.1:p.His868Asp
|
|
XM_011522424.1:c.2740C>G
|
XP_011520726.1:p.His914Asp
|
|
XM_011522425.1:c.2059C>G
|
XP_011520727.1:p.His687Asp
|
|
XM_011522426.1:c.1813C>G
|
XP_011520728.1:p.His605Asp
|
|
XM_011522427.1:c.1252C>G
|
XP_011520729.1:p.His418Asp
|
|
XR_932805.1:n.2761C>G
|
|
|
XM_011522424.3:c.2740C>G
|
XP_011520726.1:p.His914Asp
|
|
XM_017023043.2:c.1813C>G
|
XP_016878532.1:p.His605Asp
|
|
NM_005236.3:c.2602C>G
MANE Select
|
NP_005227.1:p.His868Asp
|
|