ENST00000405460.9:c.12252T>A
MANE Select
|
ENSP00000384582.2:p.Leu4084=
|
|
ENST00000425867.3:c.1206T>A
|
ENSP00000392618.3:p.Leu402=
|
|
ENST00000639431.1:c.265+87227T>A
|
ENSP00000491057.1:n.265+87227T>A
|
|
ENST00000640464.1:n.2671T>A
|
|
|
ENST00000640729.1:n.829T>A
|
|
|
ENST00000405460.6:c.12252T>A
|
ENSP00000384582.2:p.Leu4084=
|
|
NM_032119.3:c.12252T>A
|
NP_115495.3:p.Leu4084=
|
|
NR_003149.1:n.12265T>A
|
|
|
XM_011543675.1:c.12249T>A
|
XP_011541977.1:p.Leu4083=
|
|
XM_011543676.1:c.12171T>A
|
XP_011541978.1:p.Leu4057=
|
|
XM_011543677.1:c.9555T>A
|
XP_011541979.1:p.Leu3185=
|
|
XM_011543678.1:c.12252T>A
|
XP_011541980.1:p.Leu4084=
|
|
NM_032119.4:c.12252T>A
MANE Select
|
NP_115495.3:p.Leu4084=
|
|
XM_017009963.2:c.12273T>A
|
XP_016865452.1:p.Leu4091=
|
|
XM_017009964.2:c.12270T>A
|
XP_016865453.1:p.Leu4090=
|
|
XM_017009965.1:c.12270T>A
|
XP_016865454.1:p.Leu4090=
|
|
XM_017009966.2:c.12192T>A
|
XP_016865455.1:p.Leu4064=
|
|
XM_017009967.1:c.12177T>A
|
XP_016865456.1:p.Leu4059=
|
|
XM_017009968.2:c.12273T>A
|
XP_016865457.1:p.Leu4091=
|
|
XM_017009969.2:c.12273T>A
|
XP_016865458.1:p.Leu4091=
|
|
XM_017009970.2:c.12273T>A
|
XP_016865459.1:p.Leu4091=
|
|
XM_017009971.2:c.12273T>A
|
XP_016865460.1:p.Leu4091=
|
|
XM_017009972.1:c.5391T>A
|
XP_016865461.1:p.Leu1797=
|
|
XM_017009973.1:c.5370T>A
|
XP_016865462.1:p.Leu1790=
|
|
NR_003149.2:n.12268T>A
|
|
|