ENST00000318388.11:c.510T>C
(NDUFV2)
MANE Select
|
ENSP00000327268.6:p.Thr170=
|
|
ENST00000318388.10:c.510T>C
(NDUFV2)
|
ENSP00000327268.6:p.Thr170=
|
|
ENST00000400033.1:c.519T>C
(NDUFV2)
|
ENSP00000382908.1:p.Thr173=
|
|
ENST00000465096.5:n.328T>C
(NDUFV2)
|
|
|
NM_021074.4:c.510T>C
(NDUFV2)
|
NP_066552.2:p.Thr170=
|
|
NR_110771.1:n.654-3458A>G
(NDUFV2-AS1)
|
|
|
NR_110772.1:n.478-3458A>G
(NDUFV2-AS1)
|
|
|
XR_243808.1:n.612T>C
(NDUFV2)
|
|
|
XM_017025782.1:c.423T>C
(NDUFV2)
|
XP_016881271.1:p.Thr141=
|
|
XR_002958175.1:n.2804T>C
(NDUFV2)
|
|
|
XR_243808.3:n.527T>C
(NDUFV2)
|
|
|
NM_021074.5:c.510T>C
(NDUFV2)
MANE Select
|
NP_066552.2:p.Thr170=
|
|