ENST00000378802.5:c.1499G>T
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Gly500Val
|
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ENST00000378802.4:c.1499G>T
(CYP4V2)
|
ENSP00000368079.4:p.Gly500Val
|
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ENST00000502665.1:n.734G>T
(CYP4V2)
|
|
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ENST00000507209.5:n.6197G>T
(CYP4V2)
|
|
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ENST00000511608.5:c.201+1290G>T
(KLKB1)
|
|
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ENST00000513354.5:n.589G>T
(CYP4V2)
|
|
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NM_207352.3:c.1499G>T
(CYP4V2)
|
NP_997235.3:p.Gly500Val
|
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XM_005262935.2:c.1496G>T
(CYP4V2)
|
XP_005262992.1:p.Gly499Val
|
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XM_006714184.2:c.1103G>T
(CYP4V2)
|
XP_006714247.1:p.Gly368Val
|
|
XM_005262935.4:c.1496G>T
(CYP4V2)
|
XP_005262992.1:p.Gly499Val
|
|
XM_017008037.1:c.1103G>T
(CYP4V2)
|
XP_016863526.1:p.Gly368Val
|
|
NM_207352.4:c.1499G>T
(CYP4V2)
MANE Select
|
NP_997235.3:p.Gly500Val
|
|