ENST00000296589.9:c.1156+162G>A
MANE Select
|
ENSP00000296589.4:n.1156+162G>A
|
|
ENST00000296589.8:c.1156+162G>A
|
ENSP00000296589.4:n.1156+162G>A
|
|
ENST00000382102.7:c.1156+162G>A
|
ENSP00000371534.3:n.1156+162G>A
|
|
ENST00000510600.1:c.631+162G>A
|
ENSP00000424010.1:n.631+162G>A
|
|
NM_001012509.3:c.1156+162G>A
|
NP_001012527.1:n.1156+162G>A
|
|
NM_016180.4:c.1156+162G>A
|
NP_057264.3:n.1156+162G>A
|
|
XM_011514051.1:c.754+162G>A
|
XP_011512353.1:n.754+162G>A
|
|
XR_925620.1:n.1973+162G>A
|
|
|
NM_016180.5:c.1156+162G>A
MANE Select
|
NP_057264.4:n.1156+162G>A
|
|
NM_001012509.4:c.1156+162G>A
|
NP_001012527.2:n.1156+162G>A
|
|
NM_001297417.4:c.*260G>A
|
NP_001284346.2:n.*260G>A
|
|