ENST00000258145.8:c.1156C>T
MANE Select
|
ENSP00000258145.3:p.Leu386=
|
|
ENST00000258145.7:c.1156C>T
|
ENSP00000258145.3:p.Leu386=
|
|
ENST00000418919.6:c.988C>T
|
ENSP00000413130.2:p.Leu330=
|
|
ENST00000537823.1:n.155C>T
|
|
|
ENST00000540196.5:c.557-5887C>T
|
|
|
ENST00000540883.1:n.219C>T
|
|
|
ENST00000541781.5:n.1211C>T
|
|
|
ENST00000542058.5:c.1096C>T
|
ENSP00000444819.1:p.Leu366=
|
|
ENST00000543646.5:c.1252C>T
|
ENSP00000438497.1:p.Leu418=
|
|
NM_002076.3:c.1156C>T
|
NP_002067.1:p.Leu386=
|
|
NM_002076.4:c.1156C>T
MANE Select
|
NP_002067.1:p.Leu386=
|
|