ENST00000394867.9:n.1584G>A
|
|
|
ENST00000688002.1:n.3296G>A
|
|
|
ENST00000688751.1:n.281G>A
|
|
|
ENST00000689792.1:n.1049G>A
|
|
|
ENST00000262948.10:c.1145G>A
MANE Select
|
ENSP00000262948.4:p.Trp382Ter
|
|
ENST00000262948.9:c.1145G>A
|
ENSP00000262948.3:p.Trp382Ter
|
|
ENST00000394867.8:c.854G>A
|
ENSP00000378336.1:p.Trp285Ter
|
|
ENST00000597263.5:n.330G>A
|
|
|
ENST00000599021.1:c.255G>A
|
|
|
ENST00000600584.5:n.2594G>A
|
|
|
ENST00000601786.5:n.1446G>A
|
|
|
NM_030662.3:c.1145G>A , LRG_750t1:c.1145G>A
|
NP_109587.1:p.Trp382Ter
|
|
XM_006722799.2:c.866G>A
|
XP_006722862.1:p.Trp289Ter
|
|
XM_011528133.1:c.575G>A
|
XP_011526435.1:p.Trp192Ter
|
|
NM_030662.4:c.1145G>A
MANE Select
|
NP_109587.1:p.Trp382Ter
|
|