ENST00000394867.9:n.1627G>C
|
|
|
ENST00000688002.1:n.3339G>C
|
|
|
ENST00000688751.1:n.324G>C
|
|
|
ENST00000689792.1:n.1092G>C
|
|
|
ENST00000262948.10:c.1188G>C
MANE Select
|
ENSP00000262948.4:p.Thr396=
|
|
ENST00000262948.9:c.1188G>C
|
ENSP00000262948.3:p.Thr396=
|
|
ENST00000394867.8:c.897G>C
|
ENSP00000378336.1:p.Thr299=
|
|
ENST00000597263.5:n.373G>C
|
|
|
ENST00000599021.1:c.298G>C
|
|
|
ENST00000600584.5:n.2637G>C
|
|
|
ENST00000601786.5:n.1489G>C
|
|
|
NM_030662.3:c.1188G>C , LRG_750t1:c.1188G>C
|
NP_109587.1:p.Thr396=
|
|
XM_006722799.2:c.909G>C
|
XP_006722862.1:p.Thr303=
|
|
XM_011528133.1:c.618G>C
|
XP_011526435.1:p.Thr206=
|
|
NM_030662.4:c.1188G>C
MANE Select
|
NP_109587.1:p.Thr396=
|
|