ENST00000698881.1:c.1090A=
|
ENSP00000514003.1:p.Thr364=
|
|
ENST00000418331.7:c.748A=
MANE Select
|
ENSP00000400010.2:p.Thr250=
|
|
ENST00000418331.6:c.748A=
|
ENSP00000400010.2:p.Thr250=
|
|
ENST00000440289.6:c.748A=
|
ENSP00000409733.2:p.Thr250=
|
|
ENST00000613246.4:c.748A=
|
ENSP00000477933.1:p.Thr250=
|
|
ENST00000615445.4:c.748A=
|
ENSP00000479342.1:p.Thr250=
|
|
NM_001098503.1:c.748A=
|
NP_001091973.1:p.Thr250=
|
|
NM_002843.3:c.748A=
|
NP_002834.3:p.Thr250=
|
|
XM_011520249.1:c.781A=
|
XP_011518551.1:p.Thr261=
|
|
XR_930883.1:n.1098A=
|
|
|
XM_017018083.1:c.826A=
|
XP_016873572.1:p.Thr276=
|
|
XM_017018084.1:c.769A=
|
XP_016873573.1:p.Thr257=
|
|
XM_017018085.1:c.700A=
|
XP_016873574.1:p.Thr234=
|
|
XR_930883.2:n.1157A=
|
|
|
NM_002843.4:c.748A=
MANE Select
|
NP_002834.3:p.Thr250=
|
|
NM_001098503.2:c.748A=
|
NP_001091973.1:p.Thr250=
|
|