ENST00000262418.12:c.477T>C
MANE Select
|
ENSP00000262418.6:p.Leu159=
|
|
ENST00000262418.10:c.477T>C
|
ENSP00000262418.6:p.Leu159=
|
|
ENST00000399246.3:c.477T>C
|
ENSP00000382190.3:p.Leu159=
|
|
ENST00000471005.5:n.411T>C
|
|
|
ENST00000497360.5:n.616T>C
|
|
|
NM_000342.3:c.477T>C
|
NP_000333.1:p.Leu159=
|
|
XM_005257593.3:c.282T>C
|
XP_005257650.1:p.Leu94=
|
|
XM_011525129.1:c.477T>C
|
XP_011523431.1:p.Leu159=
|
|
XM_011525130.1:c.477T>C
|
XP_011523432.1:p.Leu159=
|
|
XM_011525131.1:c.477T>C
|
XP_011523433.1:p.Leu159=
|
|
XM_005257593.5:c.282T>C
|
XP_005257650.1:p.Leu94=
|
|
XM_011525129.2:c.477T>C
|
XP_011523431.1:p.Leu159=
|
|
NM_000342.4:c.477T>C
MANE Select
|
NP_000333.1:p.Leu159=
|
|