ENST00000517770.2:c.2644-3835G>T
|
ENSP00000428185.2:n.2644-3835G>T
|
|
ENST00000518635.2:c.313+617G>T
|
ENSP00000431098.1:n.313+617G>T
|
|
ENST00000310430.11:c.2644-3835G>T
MANE Select
|
ENSP00000311579.6:n.2644-3835G>T
|
|
ENST00000310430.10:c.2644-3835G>T
|
ENSP00000311579.6:n.2644-3835G>T
|
|
ENST00000518281.5:c.1933-3835G>T
|
ENSP00000429890.1:n.1933-3835G>T
|
|
ENST00000518635.1:c.313+617G>T
|
ENSP00000431098.1:n.313+617G>T
|
|
ENST00000519191.1:n.202+3074G>T
|
|
|
NM_003747.2:c.2644-3835G>T
|
NP_003738.2:n.2644-3835G>T
|
|
XM_006716263.2:c.2644-3835G>T
|
XP_006716326.1:n.2644-3835G>T
|
|
XM_011543845.1:c.2644-3835G>T
|
XP_011542147.1:n.2644-3835G>T
|
|
XM_011543846.1:c.2644-3835G>T
|
XP_011542148.1:n.2644-3835G>T
|
|
XM_011543847.1:c.2332-3835G>T
|
XP_011542149.1:n.2332-3835G>T
|
|
XM_006716263.4:c.2644-3835G>T
|
XP_006716326.1:n.2644-3835G>T
|
|
XM_011543845.3:c.2644-3835G>T
|
XP_011542147.1:n.2644-3835G>T
|
|
XM_011543846.3:c.2644-3835G>T
|
XP_011542148.1:n.2644-3835G>T
|
|
NM_003747.3:c.2644-3835G>T
MANE Select
|
NP_003738.2:n.2644-3835G>T
|
|