|
ENST00000394867.9:n.1621A=
|
|
|
|
ENST00000688002.1:n.3333A=
|
|
|
|
ENST00000688751.1:n.318A=
|
|
|
|
ENST00000689792.1:n.1086A=
|
|
|
|
ENST00000262948.10:c.1182A=
MANE Select
|
ENSP00000262948.4:p.Thr394=
|
|
|
ENST00000262948.9:c.1182A=
|
ENSP00000262948.3:p.Thr394=
|
|
|
ENST00000394867.8:c.891A=
|
ENSP00000378336.1:p.Thr297=
|
|
|
ENST00000597263.5:n.367A=
|
|
|
|
ENST00000599021.1:c.292A=
|
|
|
|
ENST00000600584.5:n.2631A=
|
|
|
|
ENST00000601786.5:n.1483A=
|
|
|
|
NM_030662.3:c.1182A= , LRG_750t1:c.1182A=
|
NP_109587.1:p.Thr394=
|
|
|
XM_006722799.2:c.903A=
|
XP_006722862.1:p.Thr301=
|
|
|
XM_011528133.1:c.612A=
|
XP_011526435.1:p.Thr204=
|
|
|
NM_030662.4:c.1182A=
MANE Select
|
NP_109587.1:p.Thr394=
|
|
