ENST00000394867.9:n.1610C>T
|
|
|
ENST00000688002.1:n.3322C>T
|
|
|
ENST00000688751.1:n.307C>T
|
|
|
ENST00000689792.1:n.1075C>T
|
|
|
ENST00000262948.10:c.1171C>T
MANE Select
|
ENSP00000262948.4:p.Gln391Ter
|
|
ENST00000262948.9:c.1171C>T
|
ENSP00000262948.3:p.Gln391Ter
|
|
ENST00000394867.8:c.880C>T
|
ENSP00000378336.1:p.Gln294Ter
|
|
ENST00000597263.5:n.356C>T
|
|
|
ENST00000599021.1:c.281C>T
|
|
|
ENST00000600584.5:n.2620C>T
|
|
|
ENST00000601786.5:n.1472C>T
|
|
|
NM_030662.3:c.1171C>T , LRG_750t1:c.1171C>T
|
NP_109587.1:p.Gln391Ter
|
|
XM_006722799.2:c.892C>T
|
XP_006722862.1:p.Gln298Ter
|
|
XM_011528133.1:c.601C>T
|
XP_011526435.1:p.Gln201Ter
|
|
NM_030662.4:c.1171C>T
MANE Select
|
NP_109587.1:p.Gln391Ter
|
|