ENST00000321998.10:c.20C>G
(COQ7)
MANE Select
|
ENSP00000322316.5:p.Ala7Gly
|
|
ENST00000321998.9:c.20C>G
(COQ7)
|
ENSP00000322316.5:p.Ala7Gly
|
|
ENST00000564746.1:n.39C>G
(COQ7)
|
|
|
ENST00000566049.5:c.20C>G
(COQ7)
|
ENSP00000456490.1:p.Ala7Gly
|
|
ENST00000566110.5:c.-239C>G
(COQ7)
|
ENSP00000456943.1:n.-239C>G
|
|
ENST00000568985.5:c.20C>G
(COQ7)
|
ENSP00000456734.1:p.Ala7Gly
|
|
ENST00000569312.5:c.20C>G
(COQ7)
|
ENSP00000459076.1:p.Ala7Gly
|
|
NM_016138.4:c.20C>G
(COQ7)
|
NP_057222.2:p.Ala7Gly
|
|
NR_119379.1:n.8G>C
(COQ7-DT)
|
|
|
NR_119380.1:n.8G>C
(COQ7-DT)
|
|
|
NR_119381.1:n.8G>C
(COQ7-DT)
|
|
|
XR_950722.1:n.90C>G
(COQ7)
|
|
|
XR_950722.3:n.90C>G
(COQ7)
|
|
|
NM_016138.5:c.20C>G
(COQ7)
MANE Select
|
NP_057222.2:p.Ala7Gly
|
|
NM_001370490.1:c.20C>G
(COQ7)
|
NP_001357419.1:p.Ala7Gly
|
|
NR_163448.1:n.71C>G
(COQ7)
|
|
|
NR_163450.1:n.71C>G
(COQ7)
|
|
|