ENST00000378802.5:c.1352G>T
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Gly451Val
|
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ENST00000378802.4:c.1352G>T
(CYP4V2)
|
ENSP00000368079.4:p.Gly451Val
|
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ENST00000502665.1:n.587G>T
(CYP4V2)
|
|
|
ENST00000507209.5:n.6050G>T
(CYP4V2)
|
|
|
ENST00000511608.5:c.148G>T
(KLKB1)
|
|
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ENST00000513354.5:n.442G>T
(CYP4V2)
|
|
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NM_207352.3:c.1352G>T
(CYP4V2)
|
NP_997235.3:p.Gly451Val
|
|
XM_005262935.2:c.1349G>T
(CYP4V2)
|
XP_005262992.1:p.Gly450Val
|
|
XM_006714184.2:c.956G>T
(CYP4V2)
|
XP_006714247.1:p.Gly319Val
|
|
XM_005262935.4:c.1349G>T
(CYP4V2)
|
XP_005262992.1:p.Gly450Val
|
|
XM_017008037.1:c.956G>T
(CYP4V2)
|
XP_016863526.1:p.Gly319Val
|
|
NM_207352.4:c.1352G>T
(CYP4V2)
MANE Select
|
NP_997235.3:p.Gly451Val
|
|