ENST00000295897.9:c.1137C>A
MANE Select
|
ENSP00000295897.4:p.Thr379=
|
|
ENST00000295897.8:c.1137C>A
|
ENSP00000295897.4:p.Thr379=
|
|
ENST00000401494.7:c.792C>A
|
ENSP00000384695.3:p.Thr264=
|
|
ENST00000415165.6:c.561C>A
|
ENSP00000401820.2:p.Thr187=
|
|
ENST00000476441.6:c.*416C>A
|
ENSP00000423727.1:n.*416C>A
|
|
ENST00000484992.1:n.457C>A
|
|
|
ENST00000503124.5:c.687C>A
|
ENSP00000421027.1:p.Thr229=
|
|
ENST00000504043.1:n.140C>A
|
|
|
ENST00000505649.5:n.823C>A
|
|
|
ENST00000509063.5:c.1137C>A
|
ENSP00000422784.1:p.Thr379=
|
|
ENST00000511370.1:c.670C>A
|
|
|
ENST00000621085.4:c.498C>A
|
ENSP00000483421.1:p.Thr166=
|
|
ENST00000621628.4:c.498C>A
|
ENSP00000480485.1:p.Thr166=
|
|
NM_000477.5:c.1137C>A
|
NP_000468.1:p.Thr379=
|
|
NM_000477.6:c.1137C>A
|
NP_000468.1:p.Thr379=
|
|
NM_000477.7:c.1137C>A
MANE Select
|
NP_000468.1:p.Thr379=
|
|