ENST00000295897.9:c.1140T>G
MANE Select
|
ENSP00000295897.4:p.Thr380=
|
|
ENST00000295897.8:c.1140T>G
|
ENSP00000295897.4:p.Thr380=
|
|
ENST00000401494.7:c.795T>G
|
ENSP00000384695.3:p.Thr265=
|
|
ENST00000415165.6:c.564T>G
|
ENSP00000401820.2:p.Thr188=
|
|
ENST00000476441.6:c.*419T>G
|
ENSP00000423727.1:n.*419T>G
|
|
ENST00000484992.1:n.460T>G
|
|
|
ENST00000503124.5:c.690T>G
|
ENSP00000421027.1:p.Thr230=
|
|
ENST00000504043.1:n.143T>G
|
|
|
ENST00000505649.5:n.826T>G
|
|
|
ENST00000509063.5:c.1140T>G
|
ENSP00000422784.1:p.Thr380=
|
|
ENST00000511370.1:c.673T>G
|
|
|
ENST00000621085.4:c.501T>G
|
ENSP00000483421.1:p.Thr167=
|
|
ENST00000621628.4:c.501T>G
|
ENSP00000480485.1:p.Thr167=
|
|
NM_000477.5:c.1140T>G
|
NP_000468.1:p.Thr380=
|
|
NM_000477.6:c.1140T>G
|
NP_000468.1:p.Thr380=
|
|
NM_000477.7:c.1140T>G
MANE Select
|
NP_000468.1:p.Thr380=
|
|