ENST00000394867.9:n.1145-27G>T
|
|
|
ENST00000687128.1:n.1145-27G>T
|
|
|
ENST00000688002.1:n.973G>T
|
|
|
ENST00000689792.1:n.646-63G>T
|
|
|
ENST00000262948.10:c.706-27G>T
MANE Select
|
ENSP00000262948.4:n.706-27G>T
|
|
ENST00000262948.9:c.706-27G>T
|
ENSP00000262948.3:n.706-27G>T
|
|
ENST00000394867.8:c.415-27G>T
|
ENSP00000378336.1:n.415-27G>T
|
|
ENST00000593364.5:n.653-27G>T
|
|
|
ENST00000595715.1:n.494G>T
|
|
|
ENST00000597263.5:n.169+1578G>T
|
|
|
ENST00000599021.1:c.29+1578G>T
|
|
|
ENST00000600584.5:n.1239G>T
|
|
|
ENST00000601786.5:n.1007-27G>T
|
|
|
ENST00000602167.5:n.426-27G>T
|
|
|
NM_030662.3:c.706-27G>T , LRG_750t1:c.706-27G>T
|
NP_109587.1:n.706-27G>T
|
|
XM_006722799.2:c.705+1578G>T
|
XP_006722862.1:n.705+1578G>T
|
|
XM_011528133.1:c.136-27G>T
|
XP_011526435.1:n.136-27G>T
|
|
XM_017026989.1:c.706-27G>T
|
XP_016882478.1:n.706-27G>T
|
|
XM_017026990.1:c.705+1578G>T
|
XP_016882479.1:n.705+1578G>T
|
|
XM_017026991.1:c.*289G>T
|
XP_016882480.1:n.*289G>T
|
|
NM_030662.4:c.706-27G>T
MANE Select
|
NP_109587.1:n.706-27G>T
|
|