ENST00000296589.9:c.-9C>A
MANE Select
|
ENSP00000296589.4:n.-9C>A
|
|
ENST00000296589.8:c.-9C>A
|
ENSP00000296589.4:n.-9C>A
|
|
ENST00000382102.7:c.-9C>A
|
ENSP00000371534.3:n.-9C>A
|
|
ENST00000509381.1:c.-9C>A
|
ENSP00000421100.1:n.-9C>A
|
|
NM_001012509.3:c.-9C>A
|
NP_001012527.1:n.-9C>A
|
|
NM_001297417.2:c.-9C>A
|
NP_001284346.2:n.-9C>A
|
|
NM_016180.4:c.-9C>A
|
NP_057264.3:n.-9C>A
|
|
XM_011514052.1:c.-9C>A
|
XP_011512354.1:n.-9C>A
|
|
XR_925620.1:n.553C>A
|
|
|
NM_016180.5:c.-9C>A
MANE Select
|
NP_057264.4:n.-9C>A
|
|
NM_001012509.4:c.-9C>A
|
NP_001012527.2:n.-9C>A
|
|
NM_001297417.3:c.-9C>A
|
NP_001284346.2:n.-9C>A
|
|
NM_001297417.4:c.-9C>A
|
NP_001284346.2:n.-9C>A
|
|