ENST00000682617.1:c.2127A=
|
ENSP00000507912.1:p.Ala709=
|
|
ENST00000683962.1:c.*1683A=
|
ENSP00000506854.1:n.*1683A=
|
|
ENST00000311895.8:c.1989A=
MANE Select
|
ENSP00000310520.7:p.Ala663=
|
|
ENST00000311895.7:c.1989A=
|
ENSP00000310520.7:p.Ala663=
|
|
ENST00000389138.7:n.1266A=
|
|
|
ENST00000462862.1:c.302A=
|
ENSP00000461322.1:n.302A=
|
|
NM_005236.2:c.1989A= , LRG_463t1:c.1989A=
|
NP_005227.1:p.Ala663=
|
|
XM_011522424.1:c.2127A=
|
XP_011520726.1:p.Ala709=
|
|
XM_011522425.1:c.1446A=
|
XP_011520727.1:p.Ala482=
|
|
XM_011522426.1:c.1200A=
|
XP_011520728.1:p.Ala400=
|
|
XM_011522427.1:c.639A=
|
XP_011520729.1:p.Ala213=
|
|
XR_932805.1:n.2148A=
|
|
|
XM_011522424.3:c.2127A=
|
XP_011520726.1:p.Ala709=
|
|
XM_017023043.2:c.1200A=
|
XP_016878532.1:p.Ala400=
|
|
NM_005236.3:c.1989A=
MANE Select
|
NP_005227.1:p.Ala663=
|
|