ENST00000372090.6:c.52+186G>A
(TOE1)
MANE Select
|
ENSP00000361162.5:n.52+186G>A
|
|
ENST00000671898.1:c.541-5979C>T
|
ENSP00000499896.1:n.541-5979C>T
|
|
ENST00000672011.1:c.-236C>T
(MUTYH)
|
ENSP00000500418.1:n.-236C>T
|
|
ENST00000372090.5:c.52+186G>A
(TOE1)
|
ENSP00000361162.5:n.52+186G>A
|
|
ENST00000471337.5:n.130+186G>A
(TOE1)
|
|
|
ENST00000477731.5:n.271+168G>A
(TOE1)
|
|
|
ENST00000495703.5:n.270G>A
(TOE1)
|
|
|
NM_025077.3:c.52+186G>A
(TOE1)
|
NP_079353.3:n.52+186G>A
|
|
XM_005270412.2:c.70+168G>A
(TOE1)
|
XP_005270469.1:n.70+168G>A
|
|
XM_005270413.3:c.-139G>A
(TOE1)
|
XP_005270470.1:n.-139G>A
|
|
XM_011540569.1:c.-233+186G>A
(TOE1)
|
XP_011538871.1:n.-233+186G>A
|
|
XR_246230.2:n.329+186G>A
(TOE1)
|
|
|
XR_426587.2:n.149+168G>A
(TOE1)
|
|
|
XR_946532.1:n.149+168G>A
(TOE1)
|
|
|
XM_005270412.4:c.70+168G>A
(TOE1)
|
XP_005270469.1:n.70+168G>A
|
|
XM_005270413.5:c.-139G>A
(TOE1)
|
XP_005270470.1:n.-139G>A
|
|
XM_011540569.3:c.-233+186G>A
(TOE1)
|
XP_011538871.1:n.-233+186G>A
|
|
XM_024452837.1:c.-139G>A
(TOE1)
|
XP_024308605.1:n.-139G>A
|
|
XR_001736951.2:n.239+186G>A
(TOE1)
|
|
|
XR_002959287.1:n.554+186G>A
(TOE1)
|
|
|
XR_246230.4:n.239+186G>A
(TOE1)
|
|
|
XR_426587.4:n.149+168G>A
(TOE1)
|
|
|
XR_946532.3:n.149+168G>A
(TOE1)
|
|
|
NM_025077.4:c.52+186G>A
(TOE1)
MANE Select
|
NP_079353.3:n.52+186G>A
|
|