ENST00000394867.9:n.1582C>T
|
|
|
ENST00000688002.1:n.3294C>T
|
|
|
ENST00000688751.1:n.279C>T
|
|
|
ENST00000689792.1:n.1047C>T
|
|
|
ENST00000262948.10:c.1143C>T
MANE Select
|
ENSP00000262948.4:p.Gly381=
|
|
ENST00000262948.9:c.1143C>T
|
ENSP00000262948.3:p.Gly381=
|
|
ENST00000394867.8:c.852C>T
|
ENSP00000378336.1:p.Gly284=
|
|
ENST00000597263.5:n.328C>T
|
|
|
ENST00000599021.1:c.253C>T
|
|
|
ENST00000600584.5:n.2592C>T
|
|
|
ENST00000601786.5:n.1444C>T
|
|
|
NM_030662.3:c.1143C>T , LRG_750t1:c.1143C>T
|
NP_109587.1:p.Gly381=
|
|
XM_006722799.2:c.864C>T
|
XP_006722862.1:p.Gly288=
|
|
XM_011528133.1:c.573C>T
|
XP_011526435.1:p.Gly191=
|
|
NM_030662.4:c.1143C>T
MANE Select
|
NP_109587.1:p.Gly381=
|
|