ENST00000352689.11:c.847+3981C>T
MANE Select
|
ENSP00000323527.6:n.847+3981C>T
|
|
ENST00000352689.10:c.847+3981C>T
|
ENSP00000323527.6:n.847+3981C>T
|
|
ENST00000421797.6:c.571+3981C>T
|
ENSP00000398094.2:n.571+3981C>T
|
|
ENST00000458153.5:c.*337+3981C>T
|
ENSP00000407705.1:n.*337+3981C>T
|
|
ENST00000494785.5:n.864+3981C>T
|
|
|
NM_001145354.1:c.778+3981C>T
|
NP_001138826.1:n.778+3981C>T
|
|
NM_013255.4:c.847+3981C>T
|
NP_037387.2:n.847+3981C>T
|
|
XM_005250356.1:c.226+3981C>T
|
XP_005250413.1:n.226+3981C>T
|
|
XM_006715993.1:c.847+3981C>T
|
XP_006716056.1:n.847+3981C>T
|
|
XM_011516224.1:c.847+3981C>T
|
XP_011514526.1:n.847+3981C>T
|
|
NM_001321316.1:c.226+3981C>T
|
NP_001308245.1:n.226+3981C>T
|
|
XM_006715993.3:c.847+3981C>T
|
XP_006716056.1:n.847+3981C>T
|
|
XM_011516224.3:c.847+3981C>T
|
XP_011514526.1:n.847+3981C>T
|
|
XM_024446766.1:c.571+3981C>T
|
XP_024302534.1:n.571+3981C>T
|
|
XM_024446767.1:c.571+3981C>T
|
XP_024302535.1:n.571+3981C>T
|
|
NM_013255.5:c.847+3981C>T
MANE Select
|
NP_037387.2:n.847+3981C>T
|
|
NM_001145354.2:c.778+3981C>T
|
NP_001138826.1:n.778+3981C>T
|
|
NM_001321316.2:c.226+3981C>T
|
NP_001308245.1:n.226+3981C>T
|
|