ENST00000296589.9:c.1126A=
MANE Select
|
ENSP00000296589.4:p.Ile376=
|
|
ENST00000296589.8:c.1126A=
|
ENSP00000296589.4:p.Ile376=
|
|
ENST00000382102.7:c.1126A=
|
ENSP00000371534.3:p.Ile376=
|
|
ENST00000509381.1:c.*68A=
|
ENSP00000421100.1:n.*68A=
|
|
ENST00000510600.1:c.601A=
|
ENSP00000424010.1:p.Ile201=
|
|
NM_001012509.3:c.1126A=
|
NP_001012527.1:p.Ile376=
|
|
NM_001297417.2:c.*68A=
|
NP_001284346.2:n.*68A=
|
|
NM_016180.4:c.1126A=
|
NP_057264.3:p.Ile376=
|
|
XM_011514051.1:c.724A=
|
XP_011512353.1:p.Ile242=
|
|
XR_925620.1:n.1943A=
|
|
|
NM_016180.5:c.1126A=
MANE Select
|
NP_057264.4:p.Ile376=
|
|
NM_001012509.4:c.1126A=
|
NP_001012527.2:p.Ile376=
|
|
NM_001297417.3:c.*68A=
|
NP_001284346.2:n.*68A=
|
|
NM_001297417.4:c.*68A=
|
NP_001284346.2:n.*68A=
|
|