|
NM_005236.3:c.2627T>A
MANE Select
|
NP_005227.1:p.Leu876Ter
|
|
ENST00000311895.8:c.2627T>A
MANE Select
|
ENSP00000310520.7:p.Leu876Ter
|
|
NM_005236.2:c.2627T>A , LRG_463t1:c.2627T>A
|
NP_005227.1:p.Leu876Ter
|
|
ENST00000311895.7:c.2627T>A
|
ENSP00000310520.7:p.Leu876Ter
|
|
ENST00000389138.7:n.1904T>A
|
|
|
ENST00000682617.1:c.2765T>A
|
ENSP00000507912.1:p.Leu922Ter
|
|
ENST00000683962.1:c.*2321T>A
|
ENSP00000506854.1:n.*2321T>A
|
|
XM_011522424.1:c.2765T>A
|
XP_011520726.1:p.Leu922Ter
|
|
XM_011522424.3:c.2765T>A
|
XP_011520726.1:p.Leu922Ter
|
|
XM_011522425.1:c.2084T>A
|
XP_011520727.1:p.Leu695Ter
|
|
XM_011522426.1:c.1838T>A
|
XP_011520728.1:p.Leu613Ter
|
|
XM_011522427.1:c.1277T>A
|
XP_011520729.1:p.Leu426Ter
|
|
XM_017023043.2:c.1838T>A
|
XP_016878532.1:p.Leu613Ter
|
|
XR_932805.1:n.2786T>A
|
|
