ENST00000378802.5:c.1473A>G
(CYP4V2)
MANE Select
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ENSP00000368079.4:p.Glu491=
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ENST00000378802.4:c.1473A>G
(CYP4V2)
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ENSP00000368079.4:p.Glu491=
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ENST00000502665.1:n.708A>G
(CYP4V2)
|
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ENST00000507209.5:n.6171A>G
(CYP4V2)
|
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ENST00000511608.5:c.201+1264A>G
(KLKB1)
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ENST00000513354.5:n.563A>G
(CYP4V2)
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NM_207352.3:c.1473A>G
(CYP4V2)
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NP_997235.3:p.Glu491=
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XM_005262935.2:c.1470A>G
(CYP4V2)
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XP_005262992.1:p.Glu490=
|
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XM_006714184.2:c.1077A>G
(CYP4V2)
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XP_006714247.1:p.Glu359=
|
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XM_005262935.4:c.1470A>G
(CYP4V2)
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XP_005262992.1:p.Glu490=
|
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XM_017008037.1:c.1077A>G
(CYP4V2)
|
XP_016863526.1:p.Glu359=
|
|
NM_207352.4:c.1473A>G
(CYP4V2)
MANE Select
|
NP_997235.3:p.Glu491=
|
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