ENST00000394867.9:n.1486-70G>C
|
|
|
ENST00000688002.1:n.3198-70G>C
|
|
|
ENST00000688751.1:n.183-70G>C
|
|
|
ENST00000689792.1:n.951-70G>C
|
|
|
ENST00000262948.10:c.1047-70G>C
MANE Select
|
ENSP00000262948.4:n.1047-70G>C
|
|
ENST00000262948.9:c.1047-70G>C
|
ENSP00000262948.3:n.1047-70G>C
|
|
ENST00000394867.8:c.756-70G>C
|
ENSP00000378336.1:n.756-70G>C
|
|
ENST00000597263.5:n.232-70G>C
|
|
|
ENST00000599021.1:c.157-70G>C
|
|
|
ENST00000600584.5:n.2426G>C
|
|
|
ENST00000601786.5:n.1348-70G>C
|
|
|
NM_030662.3:c.1047-70G>C , LRG_750t1:c.1047-70G>C
|
NP_109587.1:n.1047-70G>C
|
|
XM_006722799.2:c.768-70G>C
|
XP_006722862.1:n.768-70G>C
|
|
XM_011528133.1:c.477-70G>C
|
XP_011526435.1:n.477-70G>C
|
|
XM_017026989.1:c.1525G>C
|
XP_016882478.1:p.Gly509Arg
|
|
XM_017026990.1:c.1246G>C
|
XP_016882479.1:p.Gly416Arg
|
|
NM_030662.4:c.1047-70G>C
MANE Select
|
NP_109587.1:n.1047-70G>C
|
|