ENST00000378802.5:c.1508G>T
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Gly503Val
|
|
ENST00000378802.4:c.1508G>T
(CYP4V2)
|
ENSP00000368079.4:p.Gly503Val
|
|
ENST00000502665.1:n.743G>T
(CYP4V2)
|
|
|
ENST00000507209.5:n.6206G>T
(CYP4V2)
|
|
|
ENST00000511608.5:c.201+1299G>T
(KLKB1)
|
|
|
ENST00000513354.5:n.598G>T
(CYP4V2)
|
|
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NM_207352.3:c.1508G>T
(CYP4V2)
|
NP_997235.3:p.Gly503Val
|
|
XM_005262935.2:c.1505G>T
(CYP4V2)
|
XP_005262992.1:p.Gly502Val
|
|
XM_006714184.2:c.1112G>T
(CYP4V2)
|
XP_006714247.1:p.Gly371Val
|
|
XM_005262935.4:c.1505G>T
(CYP4V2)
|
XP_005262992.1:p.Gly502Val
|
|
XM_017008037.1:c.1112G>T
(CYP4V2)
|
XP_016863526.1:p.Gly371Val
|
|
NM_207352.4:c.1508G>T
(CYP4V2)
MANE Select
|
NP_997235.3:p.Gly503Val
|
|