ENST00000318388.11:c.732T>G
(NDUFV2)
MANE Select
|
ENSP00000327268.6:p.Gly244=
|
|
ENST00000318388.10:c.732T>G
(NDUFV2)
|
ENSP00000327268.6:p.Gly244=
|
|
ENST00000400033.1:c.741T>G
(NDUFV2)
|
ENSP00000382908.1:p.Gly247=
|
|
ENST00000465096.5:n.563T>G
(NDUFV2)
|
|
|
ENST00000474740.1:n.230T>G
(NDUFV2)
|
|
|
NM_021074.4:c.732T>G
(NDUFV2)
|
NP_066552.2:p.Gly244=
|
|
NR_110771.1:n.358-751A>C
(NDUFV2-AS1)
|
|
|
NR_110772.1:n.358-751A>C
(NDUFV2-AS1)
|
|
|
XR_243808.1:n.847T>G
(NDUFV2)
|
|
|
XM_017025782.1:c.645T>G
(NDUFV2)
|
XP_016881271.1:p.Gly215=
|
|
XR_002958175.1:n.3026T>G
(NDUFV2)
|
|
|
XR_243808.3:n.762T>G
(NDUFV2)
|
|
|
NM_021074.5:c.732T>G
(NDUFV2)
MANE Select
|
NP_066552.2:p.Gly244=
|
|