ENST00000405460.9:c.11481T>A
MANE Select
|
ENSP00000384582.2:p.Asp3827Glu
|
|
ENST00000425867.3:c.612T>A
|
ENSP00000392618.3:p.Asp204Glu
|
|
ENST00000639431.1:c.265+78877T>A
|
ENSP00000491057.1:n.265+78877T>A
|
|
ENST00000640374.1:n.4625T>A
|
|
|
ENST00000640464.1:n.1900T>A
|
|
|
ENST00000405460.6:c.11481T>A
|
ENSP00000384582.2:p.Asp3827Glu
|
|
ENST00000509621.1:c.4178T>A
|
|
|
NM_032119.3:c.11481T>A
|
NP_115495.3:p.Asp3827Glu
|
|
NR_003149.1:n.11494T>A
|
|
|
XM_011543675.1:c.11478T>A
|
XP_011541977.1:p.Asp3826Glu
|
|
XM_011543676.1:c.11400T>A
|
XP_011541978.1:p.Asp3800Glu
|
|
XM_011543677.1:c.8784T>A
|
XP_011541979.1:p.Asp2928Glu
|
|
XM_011543678.1:c.11481T>A
|
XP_011541980.1:p.Asp3827Glu
|
|
NM_032119.4:c.11481T>A
MANE Select
|
NP_115495.3:p.Asp3827Glu
|
|
XM_017009963.2:c.11502T>A
|
XP_016865452.1:p.Asp3834Glu
|
|
XM_017009964.2:c.11499T>A
|
XP_016865453.1:p.Asp3833Glu
|
|
XM_017009965.1:c.11499T>A
|
XP_016865454.1:p.Asp3833Glu
|
|
XM_017009966.2:c.11421T>A
|
XP_016865455.1:p.Asp3807Glu
|
|
XM_017009967.1:c.11406T>A
|
XP_016865456.1:p.Asp3802Glu
|
|
XM_017009968.2:c.11502T>A
|
XP_016865457.1:p.Asp3834Glu
|
|
XM_017009969.2:c.11502T>A
|
XP_016865458.1:p.Asp3834Glu
|
|
XM_017009970.2:c.11502T>A
|
XP_016865459.1:p.Asp3834Glu
|
|
XM_017009971.2:c.11502T>A
|
XP_016865460.1:p.Asp3834Glu
|
|
XM_017009972.1:c.4620T>A
|
XP_016865461.1:p.Asp1540Glu
|
|
XM_017009973.1:c.4599T>A
|
XP_016865462.1:p.Asp1533Glu
|
|
NR_003149.2:n.11497T>A
|
|
|