ENST00000405460.9:c.7580T>A
MANE Select
|
ENSP00000384582.2:p.Leu2527His
|
|
ENST00000639431.1:c.265+18127T>A
|
ENSP00000491057.1:n.265+18127T>A
|
|
ENST00000639473.1:n.3039T>A
|
|
|
ENST00000640012.1:c.1387T>A
|
|
|
ENST00000640374.1:n.724T>A
|
|
|
ENST00000640403.1:c.4871T>A
|
ENSP00000492531.1:p.Leu1624His
|
|
ENST00000640779.1:c.2309T>A
|
|
|
ENST00000405460.6:c.7580T>A
|
ENSP00000384582.2:p.Leu2527His
|
|
ENST00000509621.1:c.277T>A
|
|
|
NM_032119.3:c.7580T>A
|
NP_115495.3:p.Leu2527His
|
|
NR_003149.1:n.7593T>A
|
|
|
XM_011543675.1:c.7577T>A
|
XP_011541977.1:p.Leu2526His
|
|
XM_011543676.1:c.7499T>A
|
XP_011541978.1:p.Leu2500His
|
|
XM_011543677.1:c.4883T>A
|
XP_011541979.1:p.Leu1628His
|
|
XM_011543678.1:c.7580T>A
|
XP_011541980.1:p.Leu2527His
|
|
XM_011543679.1:c.7580T>A
|
XP_011541981.1:p.Leu2527His
|
|
NM_032119.4:c.7580T>A
MANE Select
|
NP_115495.3:p.Leu2527His
|
|
XM_017009963.2:c.7580T>A
|
XP_016865452.1:p.Leu2527His
|
|
XM_017009964.2:c.7577T>A
|
XP_016865453.1:p.Leu2526His
|
|
XM_017009965.1:c.7577T>A
|
XP_016865454.1:p.Leu2526His
|
|
XM_017009966.2:c.7499T>A
|
XP_016865455.1:p.Leu2500His
|
|
XM_017009967.1:c.7484T>A
|
XP_016865456.1:p.Leu2495His
|
|
XM_017009968.2:c.7580T>A
|
XP_016865457.1:p.Leu2527His
|
|
XM_017009969.2:c.7580T>A
|
XP_016865458.1:p.Leu2527His
|
|
XM_017009970.2:c.7580T>A
|
XP_016865459.1:p.Leu2527His
|
|
XM_017009971.2:c.7580T>A
|
XP_016865460.1:p.Leu2527His
|
|
XM_017009972.1:c.698T>A
|
XP_016865461.1:p.Leu233His
|
|
XM_017009973.1:c.698T>A
|
XP_016865462.1:p.Leu233His
|
|
XM_017009974.2:c.7580T>A
|
XP_016865463.1:p.Leu2527His
|
|
NR_003149.2:n.7596T>A
|
|
|