ENST00000295897.9:c.1596C>G
MANE Select
|
ENSP00000295897.4:p.Thr532=
|
|
ENST00000295897.8:c.1596C>G
|
ENSP00000295897.4:p.Thr532=
|
|
ENST00000401494.7:c.1251C>G
|
ENSP00000384695.3:p.Thr417=
|
|
ENST00000415165.6:c.1020C>G
|
ENSP00000401820.2:p.Thr340=
|
|
ENST00000476441.6:c.*875C>G
|
ENSP00000423727.1:n.*875C>G
|
|
ENST00000486939.1:n.250C>G
|
|
|
ENST00000503124.5:c.1146C>G
|
ENSP00000421027.1:p.Thr382=
|
|
ENST00000505649.5:n.1143C>G
|
|
|
ENST00000509063.5:c.1596C>G
|
ENSP00000422784.1:p.Thr532=
|
|
ENST00000511370.1:c.1129C>G
|
|
|
ENST00000621085.4:c.957C>G
|
ENSP00000483421.1:p.Thr319=
|
|
ENST00000621628.4:c.957C>G
|
ENSP00000480485.1:p.Thr319=
|
|
NM_000477.5:c.1596C>G
|
NP_000468.1:p.Thr532=
|
|
NM_000477.6:c.1596C>G
|
NP_000468.1:p.Thr532=
|
|
NM_000477.7:c.1596C>G
MANE Select
|
NP_000468.1:p.Thr532=
|
|