ENST00000265343.10:c.2637+159G>T
MANE Select
|
ENSP00000265343.5:n.2637+159G>T
|
|
ENST00000265343.9:c.2637+159G>T
|
ENSP00000265343.5:n.2637+159G>T
|
|
ENST00000378595.7:c.*93G>T
|
ENSP00000367858.3:n.*93G>T
|
|
NM_014423.3:c.2637+159G>T
|
NP_055238.1:n.2637+159G>T
|
|
XM_005271963.3:c.2637+159G>T
|
XP_005272020.1:n.2637+159G>T
|
|
XM_005271964.3:c.1503+159G>T
|
XP_005272021.1:n.1503+159G>T
|
|
XM_006714587.2:c.2550+159G>T
|
XP_006714650.1:n.2550+159G>T
|
|
XM_005271963.5:c.2637+159G>T
|
XP_005272020.1:n.2637+159G>T
|
|
XM_005271964.4:c.1503+159G>T
|
XP_005272021.1:n.1503+159G>T
|
|
XM_006714587.4:c.2550+159G>T
|
XP_006714650.1:n.2550+159G>T
|
|
NM_014423.4:c.2637+159G>T
MANE Select
|
NP_055238.1:n.2637+159G>T
|
|