ENST00000682568.1:n.1789C>G
|
|
|
ENST00000682617.1:c.1849C>G
|
ENSP00000507912.1:p.His617Asp
|
|
ENST00000682826.1:c.*1025C>G
|
ENSP00000507274.1:n.*1025C>G
|
|
ENST00000682909.1:n.3751C>G
|
|
|
ENST00000683277.1:n.3356C>G
|
|
|
ENST00000683407.1:n.1719C>G
|
|
|
ENST00000683962.1:c.*1405C>G
|
ENSP00000506854.1:n.*1405C>G
|
|
ENST00000311895.8:c.1711C>G
MANE Select
|
ENSP00000310520.7:p.His571Asp
|
|
ENST00000311895.7:c.1711C>G
|
ENSP00000310520.7:p.His571Asp
|
|
ENST00000389138.7:n.988C>G
|
|
|
NM_005236.2:c.1711C>G , LRG_463t1:c.1711C>G
|
NP_005227.1:p.His571Asp
|
|
XM_011522424.1:c.1849C>G
|
XP_011520726.1:p.His617Asp
|
|
XM_011522425.1:c.1168C>G
|
XP_011520727.1:p.His390Asp
|
|
XM_011522426.1:c.922C>G
|
XP_011520728.1:p.His308Asp
|
|
XM_011522427.1:c.361C>G
|
XP_011520729.1:p.His121Asp
|
|
XR_932805.1:n.1870C>G
|
|
|
XM_011522424.3:c.1849C>G
|
XP_011520726.1:p.His617Asp
|
|
XM_017023043.2:c.922C>G
|
XP_016878532.1:p.His308Asp
|
|
NM_005236.3:c.1711C>G
MANE Select
|
NP_005227.1:p.His571Asp
|
|