ENST00000296589.9:c.786A>C
MANE Select
|
ENSP00000296589.4:p.Ser262=
|
|
ENST00000296589.8:c.786A>C
|
ENSP00000296589.4:p.Ser262=
|
|
ENST00000382102.7:c.786A>C
|
ENSP00000371534.3:p.Ser262=
|
|
ENST00000505056.1:n.588A>C
|
|
|
ENST00000509381.1:c.563-9289A>C
|
ENSP00000421100.1:n.563-9289A>C
|
|
ENST00000510600.1:c.261A>C
|
ENSP00000424010.1:p.Ser87=
|
|
NM_001012509.3:c.786A>C
|
NP_001012527.1:p.Ser262=
|
|
NM_001297417.2:c.563-9289A>C
|
NP_001284346.2:n.563-9289A>C
|
|
NM_016180.4:c.786A>C
|
NP_057264.3:p.Ser262=
|
|
XM_011514051.1:c.384A>C
|
XP_011512353.1:p.Ser128=
|
|
XM_011514052.1:c.786A>C
|
XP_011512354.1:p.Ser262=
|
|
XR_925620.1:n.1603A>C
|
|
|
NM_016180.5:c.786A>C
MANE Select
|
NP_057264.4:p.Ser262=
|
|
NM_001012509.4:c.786A>C
|
NP_001012527.2:p.Ser262=
|
|
NM_001297417.3:c.563-9289A>C
|
NP_001284346.2:n.563-9289A>C
|
|
NM_001297417.4:c.563-9289A>C
|
NP_001284346.2:n.563-9289A>C
|
|