ENST00000378802.5:c.1373T>G
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Val458Gly
|
|
ENST00000378802.4:c.1373T>G
(CYP4V2)
|
ENSP00000368079.4:p.Val458Gly
|
|
ENST00000502665.1:n.608T>G
(CYP4V2)
|
|
|
ENST00000507209.5:n.6071T>G
(CYP4V2)
|
|
|
ENST00000511608.5:c.169T>G
(KLKB1)
|
|
|
ENST00000513354.5:n.463T>G
(CYP4V2)
|
|
|
NM_207352.3:c.1373T>G
(CYP4V2)
|
NP_997235.3:p.Val458Gly
|
|
XM_005262935.2:c.1370T>G
(CYP4V2)
|
XP_005262992.1:p.Val457Gly
|
|
XM_006714184.2:c.977T>G
(CYP4V2)
|
XP_006714247.1:p.Val326Gly
|
|
XM_005262935.4:c.1370T>G
(CYP4V2)
|
XP_005262992.1:p.Val457Gly
|
|
XM_017008037.1:c.977T>G
(CYP4V2)
|
XP_016863526.1:p.Val326Gly
|
|
NM_207352.4:c.1373T>G
(CYP4V2)
MANE Select
|
NP_997235.3:p.Val458Gly
|
|