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