ENST00000318388.11:c.734T>C
(NDUFV2)
MANE Select
|
ENSP00000327268.6:p.Val245Ala
|
|
ENST00000318388.10:c.734T>C
(NDUFV2)
|
ENSP00000327268.6:p.Val245Ala
|
|
ENST00000400033.1:c.743T>C
(NDUFV2)
|
ENSP00000382908.1:p.Val248Ala
|
|
ENST00000465096.5:n.565T>C
(NDUFV2)
|
|
|
ENST00000474740.1:n.232T>C
(NDUFV2)
|
|
|
NM_021074.4:c.734T>C
(NDUFV2)
|
NP_066552.2:p.Val245Ala
|
|
NR_110771.1:n.358-753A>G
(NDUFV2-AS1)
|
|
|
NR_110772.1:n.358-753A>G
(NDUFV2-AS1)
|
|
|
XR_243808.1:n.849T>C
(NDUFV2)
|
|
|
XM_017025782.1:c.647T>C
(NDUFV2)
|
XP_016881271.1:p.Val216Ala
|
|
XR_002958175.1:n.3028T>C
(NDUFV2)
|
|
|
XR_243808.3:n.764T>C
(NDUFV2)
|
|
|
NM_021074.5:c.734T>C
(NDUFV2)
MANE Select
|
NP_066552.2:p.Val245Ala
|
|