ENST00000268379.9:c.1047+29C>T
(UQCRC2)
MANE Select
|
ENSP00000268379.4:n.1047+29C>T
|
|
ENST00000268379.8:c.1047+29C>T
(UQCRC2)
|
ENSP00000268379.4:n.1047+29C>T
|
|
ENST00000561553.5:c.1047+29C>T
(UQCRC2)
|
ENSP00000456232.1:n.1047+29C>T
|
|
ENST00000563711.5:n.1227+29C>T
(UQCRC2)
|
|
|
ENST00000563898.5:c.966+1883C>T
(UQCRC2)
|
ENSP00000456738.1:n.966+1883C>T
|
|
NM_003366.2:c.1047+29C>T
(UQCRC2)
|
NP_003357.2:n.1047+29C>T
|
|
NM_003366.3:c.1047+29C>T
(UQCRC2)
|
NP_003357.2:n.1047+29C>T
|
|
XM_011545785.1:c.786+10271G>A
(PDZD9)
|
XP_011544087.1:n.786+10271G>A
|
|
XM_011545785.3:c.786+10271G>A
(PDZD9)
|
XP_011544087.1:n.786+10271G>A
|
|
XM_017023109.1:c.606+10271G>A
(PDZD9)
|
XP_016878598.1:n.606+10271G>A
|
|
XM_017023110.1:c.600+10271G>A
(PDZD9)
|
XP_016878599.1:n.600+10271G>A
|
|
NM_003366.4:c.1047+29C>T
(UQCRC2)
MANE Select
|
NP_003357.2:n.1047+29C>T
|
|