ENST00000394867.9:n.1145-42T>C
|
|
|
ENST00000687128.1:n.1145-42T>C
|
|
|
ENST00000688002.1:n.958T>C
|
|
|
ENST00000689792.1:n.646-78T>C
|
|
|
ENST00000262948.10:c.706-42T>C
MANE Select
|
ENSP00000262948.4:n.706-42T>C
|
|
ENST00000262948.9:c.706-42T>C
|
ENSP00000262948.3:n.706-42T>C
|
|
ENST00000394867.8:c.415-42T>C
|
ENSP00000378336.1:n.415-42T>C
|
|
ENST00000593364.5:n.653-42T>C
|
|
|
ENST00000595715.1:n.479T>C
|
|
|
ENST00000597263.5:n.169+1563T>C
|
|
|
ENST00000599021.1:c.29+1563T>C
|
|
|
ENST00000600584.5:n.1224T>C
|
|
|
ENST00000601786.5:n.1007-42T>C
|
|
|
ENST00000602167.5:n.426-42T>C
|
|
|
NM_030662.3:c.706-42T>C , LRG_750t1:c.706-42T>C
|
NP_109587.1:n.706-42T>C
|
|
XM_006722799.2:c.705+1563T>C
|
XP_006722862.1:n.705+1563T>C
|
|
XM_011528133.1:c.136-42T>C
|
XP_011526435.1:n.136-42T>C
|
|
XM_017026989.1:c.706-42T>C
|
XP_016882478.1:n.706-42T>C
|
|
XM_017026990.1:c.705+1563T>C
|
XP_016882479.1:n.705+1563T>C
|
|
XM_017026991.1:c.*274T>C
|
XP_016882480.1:n.*274T>C
|
|
NM_030662.4:c.706-42T>C
MANE Select
|
NP_109587.1:n.706-42T>C
|
|