ENST00000295897.9:c.1111C>T
MANE Select
|
ENSP00000295897.4:p.Leu371=
|
|
ENST00000295897.8:c.1111C>T
|
ENSP00000295897.4:p.Leu371=
|
|
ENST00000401494.7:c.766C>T
|
ENSP00000384695.3:p.Leu256=
|
|
ENST00000415165.6:c.535C>T
|
ENSP00000401820.2:p.Leu179=
|
|
ENST00000476441.6:c.*390C>T
|
ENSP00000423727.1:n.*390C>T
|
|
ENST00000484992.1:n.431C>T
|
|
|
ENST00000503124.5:c.661C>T
|
ENSP00000421027.1:p.Leu221=
|
|
ENST00000504043.1:n.114C>T
|
|
|
ENST00000505649.5:n.797C>T
|
|
|
ENST00000509063.5:c.1111C>T
|
ENSP00000422784.1:p.Leu371=
|
|
ENST00000511370.1:c.644C>T
|
|
|
ENST00000621085.4:c.491-19C>T
|
ENSP00000483421.1:n.491-19C>T
|
|
ENST00000621628.4:c.487-15C>T
|
ENSP00000480485.1:n.487-15C>T
|
|
NM_000477.5:c.1111C>T
|
NP_000468.1:p.Leu371=
|
|
NM_000477.6:c.1111C>T
|
NP_000468.1:p.Leu371=
|
|
NM_000477.7:c.1111C>T
MANE Select
|
NP_000468.1:p.Leu371=
|
|