ENST00000682617.1:c.2467C>T
|
ENSP00000507912.1:p.Gln823Ter
|
|
ENST00000683962.1:c.*2023C>T
|
ENSP00000506854.1:n.*2023C>T
|
|
ENST00000311895.8:c.2329C>T
MANE Select
|
ENSP00000310520.7:p.Gln777Ter
|
|
ENST00000311895.7:c.2329C>T
|
ENSP00000310520.7:p.Gln777Ter
|
|
ENST00000389138.7:n.1606C>T
|
|
|
ENST00000462862.1:c.642C>T
|
ENSP00000461322.1:n.642C>T
|
|
NM_005236.2:c.2329C>T , LRG_463t1:c.2329C>T
|
NP_005227.1:p.Gln777Ter
|
|
XM_011522424.1:c.2467C>T
|
XP_011520726.1:p.Gln823Ter
|
|
XM_011522425.1:c.1786C>T
|
XP_011520727.1:p.Gln596Ter
|
|
XM_011522426.1:c.1540C>T
|
XP_011520728.1:p.Gln514Ter
|
|
XM_011522427.1:c.979C>T
|
XP_011520729.1:p.Gln327Ter
|
|
XR_932805.1:n.2488C>T
|
|
|
XM_011522424.3:c.2467C>T
|
XP_011520726.1:p.Gln823Ter
|
|
XM_017023043.2:c.1540C>T
|
XP_016878532.1:p.Gln514Ter
|
|
NM_005236.3:c.2329C>T
MANE Select
|
NP_005227.1:p.Gln777Ter
|
|