ENST00000405460.9:c.11400A>G
MANE Select
|
ENSP00000384582.2:p.Leu3800=
|
|
ENST00000425867.3:c.531A>G
|
ENSP00000392618.3:p.Leu177=
|
|
ENST00000639431.1:c.265+78796A>G
|
ENSP00000491057.1:n.265+78796A>G
|
|
ENST00000640374.1:n.4544A>G
|
|
|
ENST00000640464.1:n.1819A>G
|
|
|
ENST00000405460.6:c.11400A>G
|
ENSP00000384582.2:p.Leu3800=
|
|
ENST00000509621.1:c.4097A>G
|
|
|
NM_032119.3:c.11400A>G
|
NP_115495.3:p.Leu3800=
|
|
NR_003149.1:n.11413A>G
|
|
|
XM_011543675.1:c.11397A>G
|
XP_011541977.1:p.Leu3799=
|
|
XM_011543676.1:c.11319A>G
|
XP_011541978.1:p.Leu3773=
|
|
XM_011543677.1:c.8703A>G
|
XP_011541979.1:p.Leu2901=
|
|
XM_011543678.1:c.11400A>G
|
XP_011541980.1:p.Leu3800=
|
|
NM_032119.4:c.11400A>G
MANE Select
|
NP_115495.3:p.Leu3800=
|
|
XM_017009963.2:c.11421A>G
|
XP_016865452.1:p.Leu3807=
|
|
XM_017009964.2:c.11418A>G
|
XP_016865453.1:p.Leu3806=
|
|
XM_017009965.1:c.11418A>G
|
XP_016865454.1:p.Leu3806=
|
|
XM_017009966.2:c.11340A>G
|
XP_016865455.1:p.Leu3780=
|
|
XM_017009967.1:c.11325A>G
|
XP_016865456.1:p.Leu3775=
|
|
XM_017009968.2:c.11421A>G
|
XP_016865457.1:p.Leu3807=
|
|
XM_017009969.2:c.11421A>G
|
XP_016865458.1:p.Leu3807=
|
|
XM_017009970.2:c.11421A>G
|
XP_016865459.1:p.Leu3807=
|
|
XM_017009971.2:c.11421A>G
|
XP_016865460.1:p.Leu3807=
|
|
XM_017009972.1:c.4539A>G
|
XP_016865461.1:p.Leu1513=
|
|
XM_017009973.1:c.4518A>G
|
XP_016865462.1:p.Leu1506=
|
|
NR_003149.2:n.11416A>G
|
|
|