ENST00000405460.9:c.11561C>A
MANE Select
|
ENSP00000384582.2:p.Ala3854Asp
|
|
ENST00000425867.3:c.692C>A
|
ENSP00000392618.3:p.Ala231Asp
|
|
ENST00000639431.1:c.265+78957C>A
|
ENSP00000491057.1:n.265+78957C>A
|
|
ENST00000640374.1:n.4705C>A
|
|
|
ENST00000640464.1:n.1980C>A
|
|
|
ENST00000405460.6:c.11561C>A
|
ENSP00000384582.2:p.Ala3854Asp
|
|
ENST00000509621.1:c.4258C>A
|
|
|
NM_032119.3:c.11561C>A
|
NP_115495.3:p.Ala3854Asp
|
|
NR_003149.1:n.11574C>A
|
|
|
XM_011543675.1:c.11558C>A
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XP_011541977.1:p.Ala3853Asp
|
|
XM_011543676.1:c.11480C>A
|
XP_011541978.1:p.Ala3827Asp
|
|
XM_011543677.1:c.8864C>A
|
XP_011541979.1:p.Ala2955Asp
|
|
XM_011543678.1:c.11561C>A
|
XP_011541980.1:p.Ala3854Asp
|
|
NM_032119.4:c.11561C>A
MANE Select
|
NP_115495.3:p.Ala3854Asp
|
|
XM_017009963.2:c.11582C>A
|
XP_016865452.1:p.Ala3861Asp
|
|
XM_017009964.2:c.11579C>A
|
XP_016865453.1:p.Ala3860Asp
|
|
XM_017009965.1:c.11579C>A
|
XP_016865454.1:p.Ala3860Asp
|
|
XM_017009966.2:c.11501C>A
|
XP_016865455.1:p.Ala3834Asp
|
|
XM_017009967.1:c.11486C>A
|
XP_016865456.1:p.Ala3829Asp
|
|
XM_017009968.2:c.11582C>A
|
XP_016865457.1:p.Ala3861Asp
|
|
XM_017009969.2:c.11582C>A
|
XP_016865458.1:p.Ala3861Asp
|
|
XM_017009970.2:c.11582C>A
|
XP_016865459.1:p.Ala3861Asp
|
|
XM_017009971.2:c.11582C>A
|
XP_016865460.1:p.Ala3861Asp
|
|
XM_017009972.1:c.4700C>A
|
XP_016865461.1:p.Ala1567Asp
|
|
XM_017009973.1:c.4679C>A
|
XP_016865462.1:p.Ala1560Asp
|
|
NR_003149.2:n.11577C>A
|
|
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