ENST00000205402.10:c.826A=
MANE Select
|
ENSP00000205402.3:p.Thr276=
|
|
ENST00000205402.9:c.826A=
|
ENSP00000205402.3:p.Thr276=
|
|
ENST00000415325.5:c.*500A=
|
ENSP00000402593.1:n.*500A=
|
|
ENST00000417551.5:c.826A=
|
ENSP00000390667.1:p.Thr276=
|
|
ENST00000437604.6:c.682A=
|
ENSP00000387542.2:p.Thr228=
|
|
ENST00000440410.5:c.757A=
|
ENSP00000417016.1:p.Thr253=
|
|
NM_000108.4:c.826A=
|
NP_000099.2:p.Thr276=
|
|
NM_001289750.1:c.529A=
|
NP_001276679.1:p.Thr177=
|
|
NM_001289751.1:c.757A=
|
NP_001276680.1:p.Thr253=
|
|
NM_001289752.1:c.682A=
|
NP_001276681.1:p.Thr228=
|
|
NM_000108.5:c.826A=
MANE Select
|
NP_000099.2:p.Thr276=
|
|