ENST00000405460.9:c.7064C>A
MANE Select
|
ENSP00000384582.2:p.Ala2355Asp
|
|
ENST00000639431.1:c.265+16508C>A
|
ENSP00000491057.1:n.265+16508C>A
|
|
ENST00000639473.1:n.2523C>A
|
|
|
ENST00000640012.1:c.871C>A
|
|
|
ENST00000640374.1:n.208C>A
|
|
|
ENST00000640403.1:c.4355C>A
|
ENSP00000492531.1:p.Ala1452Asp
|
|
ENST00000640779.1:c.1793C>A
|
|
|
ENST00000405460.6:c.7064C>A
|
ENSP00000384582.2:p.Ala2355Asp
|
|
NM_032119.3:c.7064C>A
|
NP_115495.3:p.Ala2355Asp
|
|
NR_003149.1:n.7077C>A
|
|
|
XM_011543675.1:c.7061C>A
|
XP_011541977.1:p.Ala2354Asp
|
|
XM_011543676.1:c.6983C>A
|
XP_011541978.1:p.Ala2328Asp
|
|
XM_011543677.1:c.4367C>A
|
XP_011541979.1:p.Ala1456Asp
|
|
XM_011543678.1:c.7064C>A
|
XP_011541980.1:p.Ala2355Asp
|
|
XM_011543679.1:c.7064C>A
|
XP_011541981.1:p.Ala2355Asp
|
|
NM_032119.4:c.7064C>A
MANE Select
|
NP_115495.3:p.Ala2355Asp
|
|
XM_017009963.2:c.7064C>A
|
XP_016865452.1:p.Ala2355Asp
|
|
XM_017009964.2:c.7061C>A
|
XP_016865453.1:p.Ala2354Asp
|
|
XM_017009965.1:c.7061C>A
|
XP_016865454.1:p.Ala2354Asp
|
|
XM_017009966.2:c.6983C>A
|
XP_016865455.1:p.Ala2328Asp
|
|
XM_017009967.1:c.6968C>A
|
XP_016865456.1:p.Ala2323Asp
|
|
XM_017009968.2:c.7064C>A
|
XP_016865457.1:p.Ala2355Asp
|
|
XM_017009969.2:c.7064C>A
|
XP_016865458.1:p.Ala2355Asp
|
|
XM_017009970.2:c.7064C>A
|
XP_016865459.1:p.Ala2355Asp
|
|
XM_017009971.2:c.7064C>A
|
XP_016865460.1:p.Ala2355Asp
|
|
XM_017009972.1:c.182C>A
|
XP_016865461.1:p.Ala61Asp
|
|
XM_017009973.1:c.182C>A
|
XP_016865462.1:p.Ala61Asp
|
|
XM_017009974.2:c.7064C>A
|
XP_016865463.1:p.Ala2355Asp
|
|
NR_003149.2:n.7080C>A
|
|
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