ENST00000682617.1:c.2632A=
|
ENSP00000507912.1:p.Thr878=
|
|
ENST00000683962.1:c.*2188A=
|
ENSP00000506854.1:n.*2188A=
|
|
ENST00000311895.8:c.2494A=
MANE Select
|
ENSP00000310520.7:p.Thr832=
|
|
ENST00000311895.7:c.2494A=
|
ENSP00000310520.7:p.Thr832=
|
|
ENST00000389138.7:n.1771A=
|
|
|
NM_005236.2:c.2494A= , LRG_463t1:c.2494A=
|
NP_005227.1:p.Thr832=
|
|
XM_011522424.1:c.2632A=
|
XP_011520726.1:p.Thr878=
|
|
XM_011522425.1:c.1951A=
|
XP_011520727.1:p.Thr651=
|
|
XM_011522426.1:c.1705A=
|
XP_011520728.1:p.Thr569=
|
|
XM_011522427.1:c.1144A=
|
XP_011520729.1:p.Thr382=
|
|
XR_932805.1:n.2653A=
|
|
|
XM_011522424.3:c.2632A=
|
XP_011520726.1:p.Thr878=
|
|
XM_017023043.2:c.1705A=
|
XP_016878532.1:p.Thr569=
|
|
NM_005236.3:c.2494A=
MANE Select
|
NP_005227.1:p.Thr832=
|
|