ENST00000403733.8:c.3142-122C>G
MANE Select
|
ENSP00000384222.3:n.3142-122C>G
|
|
ENST00000403733.7:c.3142-122C>G
|
ENSP00000384222.3:n.3142-122C>G
|
|
ENST00000427431.5:c.*2534-122C>G
|
ENSP00000393342.1:n.*2534-122C>G
|
|
ENST00000438543.5:c.*938-122C>G
|
ENSP00000413521.1:n.*938-122C>G
|
|
ENST00000448232.6:c.3214-122C>G
|
ENSP00000398577.2:n.3214-122C>G
|
|
ENST00000504005.5:c.2188-122C>G
|
ENSP00000427569.1:n.2188-122C>G
|
|
ENST00000508747.1:c.526-122C>G
|
ENSP00000420835.1:n.526-122C>G
|
|
ENST00000513834.5:c.2995-122C>G
|
ENSP00000425054.1:n.2995-122C>G
|
|
NM_024949.5:c.3142-122C>G
|
NP_079225.5:n.3142-122C>G
|
|
XM_011532269.1:c.3214-122C>G
|
XP_011530571.1:n.3214-122C>G
|
|
XM_011532269.3:c.3214-122C>G
|
XP_011530571.1:n.3214-122C>G
|
|
XM_024454225.1:c.2920-122C>G
|
XP_024309993.1:n.2920-122C>G
|
|
NM_024949.6:c.3142-122C>G
MANE Select
|
NP_079225.5:n.3142-122C>G
|
|