|
NM_032119.4:c.10603G>T
MANE Select
|
NP_115495.3:p.Glu3535Ter
|
|
ENST00000405460.9:c.10603G>T
MANE Select
|
ENSP00000384582.2:p.Glu3535Ter
|
|
NM_032119.3:c.10603G>T
|
NP_115495.3:p.Glu3535Ter
|
|
NR_003149.1:n.10616G>T
|
|
|
NR_003149.2:n.10619G>T
|
|
|
ENST00000405460.6:c.10603G>T
|
ENSP00000384582.2:p.Glu3535Ter
|
|
ENST00000509621.1:c.3300G>T
|
|
|
ENST00000639431.1:c.265+68890G>T
|
ENSP00000491057.1:n.265+68890G>T
|
|
ENST00000640374.1:n.3747G>T
|
|
|
ENST00000640464.1:n.1022G>T
|
|
|
XM_011543675.1:c.10600G>T
|
XP_011541977.1:p.Glu3534Ter
|
|
XM_011543676.1:c.10522G>T
|
XP_011541978.1:p.Glu3508Ter
|
|
XM_011543677.1:c.7906G>T
|
XP_011541979.1:p.Glu2636Ter
|
|
XM_011543678.1:c.10603G>T
|
XP_011541980.1:p.Glu3535Ter
|
|
XM_011543679.1:c.10603G>T
|
XP_011541981.1:p.Glu3535Ter
|
|
XM_017009963.2:c.10624G>T
|
XP_016865452.1:p.Glu3542Ter
|
|
XM_017009964.2:c.10621G>T
|
XP_016865453.1:p.Glu3541Ter
|
|
XM_017009965.1:c.10621G>T
|
XP_016865454.1:p.Glu3541Ter
|
|
XM_017009966.2:c.10543G>T
|
XP_016865455.1:p.Glu3515Ter
|
|
XM_017009967.1:c.10528G>T
|
XP_016865456.1:p.Glu3510Ter
|
|
XM_017009968.2:c.10624G>T
|
XP_016865457.1:p.Glu3542Ter
|
|
XM_017009969.2:c.10624G>T
|
XP_016865458.1:p.Glu3542Ter
|
|
XM_017009970.2:c.10624G>T
|
XP_016865459.1:p.Glu3542Ter
|
|
XM_017009971.2:c.10624G>T
|
XP_016865460.1:p.Glu3542Ter
|
|
XM_017009972.1:c.3742G>T
|
XP_016865461.1:p.Glu1248Ter
|
|
XM_017009973.1:c.3721G>T
|
XP_016865462.1:p.Glu1241Ter
|
|
XM_017009974.2:c.10624G>T
|
XP_016865463.1:p.Glu3542Ter
|