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NM_014363.6:c.11780C>T
MANE Select
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NP_055178.3:p.Ala3927Val
|
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ENST00000382292.9:c.11780C>T
MANE Select
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ENSP00000371729.3:p.Ala3927Val
|
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NM_001278055.1:c.11339C>T
|
NP_001264984.1:p.Ala3780Val
|
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NM_001278055.2:c.11339C>T
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NP_001264984.1:p.Ala3780Val
|
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NM_014363.5:c.11780C>T
|
NP_055178.3:p.Ala3927Val
|
|
ENST00000382292.7:c.11780C>T
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ENSP00000371729.3:p.Ala3927Val
|
|
ENST00000382298.7:c.11780C>T
|
ENSP00000371735.3:p.Ala3927Val
|
|
ENST00000402364.1:c.9530C>T
|
ENSP00000385844.1:p.Ala3177Val
|
|
ENST00000423156.1:c.1058-2612C>T
|
ENSP00000390925.1:n.1058-2612C>T
|
|
ENST00000423156.2:c.2186-2612C>T
|
ENSP00000390925.2:n.2186-2612C>T
|
|
ENST00000455470.5:c.2130-2612C>T
|
|
|
ENST00000455470.6:c.2432-2612C>T
|
ENSP00000406565.2:n.2432-2612C>T
|
|
ENST00000682775.1:c.2186-19981C>T
|
ENSP00000508399.1:n.2186-19981C>T
|
|
ENST00000682944.1:c.11807C>T
|
ENSP00000507173.1:p.Ala3936Val
|
|
ENST00000683210.1:c.2185+21689C>T
|
ENSP00000506739.1:n.2185+21689C>T
|
|
ENST00000683270.1:c.6446-2612C>T
|
ENSP00000507624.1:n.6446-2612C>T
|
|
ENST00000683367.1:c.2177-2612C>T
|
ENSP00000507780.1:n.2177-2612C>T
|
|
ENST00000683489.1:c.2292-2144C>T
|
ENSP00000508403.1:n.2292-2144C>T
|
|
ENST00000683680.1:c.2319-2144C>T
|
ENSP00000507223.1:n.2319-2144C>T
|
|
ENST00000684163.1:c.2204-2612C>T
|
ENSP00000508262.1:n.2204-2612C>T
|
|
ENST00000684196.1:n.4543-2612C>T
|
|
|
ENST00000684325.1:c.2186-10422C>T
|
ENSP00000508121.1:n.2186-10422C>T
|
|
ENST00000684385.1:c.2221-2612C>T
|
ENSP00000507855.1:n.2221-2612C>T
|
|
ENST00000684497.1:c.2186-9452C>T
|
ENSP00000507057.1:n.2186-9452C>T
|
|
XM_005266338.1:c.11807C>T
|
XP_005266395.1:p.Ala3936Val
|
|
XM_005266338.2:c.11807C>T
|
XP_005266395.1:p.Ala3936Val
|
|
XM_011535038.1:c.11831C>T
|
XP_011533340.1:p.Ala3944Val
|
|
XM_011535039.1:c.11798C>T
|
XP_011533341.1:p.Ala3933Val
|
|
XM_011535039.2:c.11798C>T
|
XP_011533341.1:p.Ala3933Val
|
|
XM_017020539.1:c.11771C>T
|
XP_016876028.1:p.Ala3924Val
|
|
XM_024449337.1:c.11807C>T
|
XP_024305105.1:p.Ala3936Val
|