ENST00000405460.9:c.11480A>T
MANE Select
|
ENSP00000384582.2:p.Asp3827Val
|
|
ENST00000425867.3:c.611A>T
|
ENSP00000392618.3:p.Asp204Val
|
|
ENST00000639431.1:c.265+78876A>T
|
ENSP00000491057.1:n.265+78876A>T
|
|
ENST00000640374.1:n.4624A>T
|
|
|
ENST00000640464.1:n.1899A>T
|
|
|
ENST00000405460.6:c.11480A>T
|
ENSP00000384582.2:p.Asp3827Val
|
|
ENST00000509621.1:c.4177A>T
|
|
|
NM_032119.3:c.11480A>T
|
NP_115495.3:p.Asp3827Val
|
|
NR_003149.1:n.11493A>T
|
|
|
XM_011543675.1:c.11477A>T
|
XP_011541977.1:p.Asp3826Val
|
|
XM_011543676.1:c.11399A>T
|
XP_011541978.1:p.Asp3800Val
|
|
XM_011543677.1:c.8783A>T
|
XP_011541979.1:p.Asp2928Val
|
|
XM_011543678.1:c.11480A>T
|
XP_011541980.1:p.Asp3827Val
|
|
NM_032119.4:c.11480A>T
MANE Select
|
NP_115495.3:p.Asp3827Val
|
|
XM_017009963.2:c.11501A>T
|
XP_016865452.1:p.Asp3834Val
|
|
XM_017009964.2:c.11498A>T
|
XP_016865453.1:p.Asp3833Val
|
|
XM_017009965.1:c.11498A>T
|
XP_016865454.1:p.Asp3833Val
|
|
XM_017009966.2:c.11420A>T
|
XP_016865455.1:p.Asp3807Val
|
|
XM_017009967.1:c.11405A>T
|
XP_016865456.1:p.Asp3802Val
|
|
XM_017009968.2:c.11501A>T
|
XP_016865457.1:p.Asp3834Val
|
|
XM_017009969.2:c.11501A>T
|
XP_016865458.1:p.Asp3834Val
|
|
XM_017009970.2:c.11501A>T
|
XP_016865459.1:p.Asp3834Val
|
|
XM_017009971.2:c.11501A>T
|
XP_016865460.1:p.Asp3834Val
|
|
XM_017009972.1:c.4619A>T
|
XP_016865461.1:p.Asp1540Val
|
|
XM_017009973.1:c.4598A>T
|
XP_016865462.1:p.Asp1533Val
|
|
NR_003149.2:n.11496A>T
|
|
|