ENST00000205402.10:c.843T>A
MANE Select
|
ENSP00000205402.3:p.Ala281=
|
|
ENST00000205402.9:c.843T>A
|
ENSP00000205402.3:p.Ala281=
|
|
ENST00000415325.5:c.*517T>A
|
ENSP00000402593.1:n.*517T>A
|
|
ENST00000417551.5:c.843T>A
|
ENSP00000390667.1:p.Ala281=
|
|
ENST00000437604.6:c.699T>A
|
ENSP00000387542.2:p.Ala233=
|
|
ENST00000440410.5:c.774T>A
|
ENSP00000417016.1:p.Ala258=
|
|
NM_000108.4:c.843T>A
|
NP_000099.2:p.Ala281=
|
|
NM_001289750.1:c.546T>A
|
NP_001276679.1:p.Ala182=
|
|
NM_001289751.1:c.774T>A
|
NP_001276680.1:p.Ala258=
|
|
NM_001289752.1:c.699T>A
|
NP_001276681.1:p.Ala233=
|
|
NM_000108.5:c.843T>A
MANE Select
|
NP_000099.2:p.Ala281=
|
|