ENST00000403733.8:c.3384+136T>C
MANE Select
|
ENSP00000384222.3:n.3384+136T>C
|
|
ENST00000403733.7:c.3384+136T>C
|
ENSP00000384222.3:n.3384+136T>C
|
|
ENST00000427431.5:c.*2776+136T>C
|
ENSP00000393342.1:n.*2776+136T>C
|
|
ENST00000438543.5:c.*1180+136T>C
|
ENSP00000413521.1:n.*1180+136T>C
|
|
ENST00000448232.6:c.3456+136T>C
|
ENSP00000398577.2:n.3456+136T>C
|
|
ENST00000504005.5:c.2430+136T>C
|
ENSP00000427569.1:n.2430+136T>C
|
|
ENST00000508747.1:c.768+136T>C
|
ENSP00000420835.1:n.768+136T>C
|
|
ENST00000513834.5:c.3237+136T>C
|
ENSP00000425054.1:n.3237+136T>C
|
|
NM_024949.5:c.3384+136T>C
|
NP_079225.5:n.3384+136T>C
|
|
XM_011532269.1:c.3456+136T>C
|
XP_011530571.1:n.3456+136T>C
|
|
XM_011532269.3:c.3456+136T>C
|
XP_011530571.1:n.3456+136T>C
|
|
XM_024454225.1:c.3162+136T>C
|
XP_024309993.1:n.3162+136T>C
|
|
NM_024949.6:c.3384+136T>C
MANE Select
|
NP_079225.5:n.3384+136T>C
|
|