|
ENST00000394867.9:n.1561G=
|
|
|
|
ENST00000688002.1:n.3273G=
|
|
|
|
ENST00000688751.1:n.258G=
|
|
|
|
ENST00000689792.1:n.1026G=
|
|
|
|
ENST00000262948.10:c.1122G=
MANE Select
|
ENSP00000262948.4:p.Val374=
|
|
|
ENST00000262948.9:c.1122G=
|
ENSP00000262948.3:p.Val374=
|
|
|
ENST00000394867.8:c.831G=
|
ENSP00000378336.1:p.Val277=
|
|
|
ENST00000597263.5:n.307G=
|
|
|
|
ENST00000599021.1:c.232G=
|
|
|
|
ENST00000600584.5:n.2571G=
|
|
|
|
ENST00000601786.5:n.1423G=
|
|
|
|
NM_030662.3:c.1122G= , LRG_750t1:c.1122G=
|
NP_109587.1:p.Val374=
|
|
|
XM_006722799.2:c.843G=
|
XP_006722862.1:p.Val281=
|
|
|
XM_011528133.1:c.552G=
|
XP_011526435.1:p.Val184=
|
|
|
NM_030662.4:c.1122G=
MANE Select
|
NP_109587.1:p.Val374=
|
|
