ENST00000405460.9:c.10841T>C
MANE Select
|
ENSP00000384582.2:p.Val3614Ala
|
|
ENST00000639431.1:c.265+69453T>C
|
ENSP00000491057.1:n.265+69453T>C
|
|
ENST00000640374.1:n.3985T>C
|
|
|
ENST00000640464.1:n.1260T>C
|
|
|
ENST00000405460.6:c.10841T>C
|
ENSP00000384582.2:p.Val3614Ala
|
|
ENST00000509621.1:c.3538T>C
|
|
|
NM_032119.3:c.10841T>C
|
NP_115495.3:p.Val3614Ala
|
|
NR_003149.1:n.10854T>C
|
|
|
XM_011543675.1:c.10838T>C
|
XP_011541977.1:p.Val3613Ala
|
|
XM_011543676.1:c.10760T>C
|
XP_011541978.1:p.Val3587Ala
|
|
XM_011543677.1:c.8144T>C
|
XP_011541979.1:p.Val2715Ala
|
|
XM_011543678.1:c.10841T>C
|
XP_011541980.1:p.Val3614Ala
|
|
XM_011543679.1:c.*63T>C
|
XP_011541981.1:n.*63T>C
|
|
NM_032119.4:c.10841T>C
MANE Select
|
NP_115495.3:p.Val3614Ala
|
|
XM_017009963.2:c.10862T>C
|
XP_016865452.1:p.Val3621Ala
|
|
XM_017009964.2:c.10859T>C
|
XP_016865453.1:p.Val3620Ala
|
|
XM_017009965.1:c.10859T>C
|
XP_016865454.1:p.Val3620Ala
|
|
XM_017009966.2:c.10781T>C
|
XP_016865455.1:p.Val3594Ala
|
|
XM_017009967.1:c.10766T>C
|
XP_016865456.1:p.Val3589Ala
|
|
XM_017009968.2:c.10862T>C
|
XP_016865457.1:p.Val3621Ala
|
|
XM_017009969.2:c.10862T>C
|
XP_016865458.1:p.Val3621Ala
|
|
XM_017009970.2:c.10862T>C
|
XP_016865459.1:p.Val3621Ala
|
|
XM_017009971.2:c.10862T>C
|
XP_016865460.1:p.Val3621Ala
|
|
XM_017009972.1:c.3980T>C
|
XP_016865461.1:p.Val1327Ala
|
|
XM_017009973.1:c.3959T>C
|
XP_016865462.1:p.Val1320Ala
|
|
XM_017009974.2:c.*63T>C
|
XP_016865463.1:n.*63T>C
|
|
NR_003149.2:n.10857T>C
|
|
|