ENST00000268379.9:c.761G>A
(UQCRC2)
MANE Select
|
ENSP00000268379.4:p.Arg254His
|
|
ENST00000268379.8:c.761G>A
(UQCRC2)
|
ENSP00000268379.4:p.Arg254His
|
|
ENST00000561553.5:c.761G>A
(UQCRC2)
|
ENSP00000456232.1:p.Arg254His
|
|
ENST00000563711.5:n.941G>A
(UQCRC2)
|
|
|
ENST00000563898.5:c.761G>A
(UQCRC2)
|
ENSP00000456738.1:p.Arg254His
|
|
ENST00000567810.1:n.315G>A
(UQCRC2)
|
|
|
NM_003366.2:c.761G>A
(UQCRC2)
|
NP_003357.2:p.Arg254His
|
|
NM_003366.3:c.761G>A
(UQCRC2)
|
NP_003357.2:p.Arg254His
|
|
XM_011545785.1:c.786+12661C>T
(PDZD9)
|
XP_011544087.1:n.786+12661C>T
|
|
XM_011545785.3:c.786+12661C>T
(PDZD9)
|
XP_011544087.1:n.786+12661C>T
|
|
XM_017023109.1:c.606+12661C>T
(PDZD9)
|
XP_016878598.1:n.606+12661C>T
|
|
XM_017023110.1:c.600+12661C>T
(PDZD9)
|
XP_016878599.1:n.600+12661C>T
|
|
NM_003366.4:c.761G>A
(UQCRC2)
MANE Select
|
NP_003357.2:p.Arg254His
|
|