ENST00000688755.1:c.928+11931G>A
(ATP1B1)
|
ENSP00000508725.1:n.928+11931G>A
|
|
ENST00000367811.8:c.1098+3534C>T
(NME7)
MANE Select
|
ENSP00000356785.3:n.1098+3534C>T
|
|
ENST00000367811.7:c.1098+3534C>T
(NME7)
|
ENSP00000356785.3:n.1098+3534C>T
|
|
ENST00000472647.5:c.990+3534C>T
(NME7)
|
ENSP00000433341.1:n.990+3534C>T
|
|
ENST00000493481.1:n.137+3520C>T
(NME7)
|
|
|
ENST00000525440.5:c.*141+3534C>T
(NME7)
|
ENSP00000431467.1:n.*141+3534C>T
|
|
ENST00000530739.5:n.68+24730C>T
(NME7)
|
|
|
NM_013330.4:c.1098+3534C>T
(NME7)
|
NP_037462.1:n.1098+3534C>T
|
|
NM_197972.2:c.990+3534C>T
(NME7)
|
NP_932076.1:n.990+3534C>T
|
|
NR_104229.1:n.1414+3534C>T
(NME7)
|
|
|
XM_005245106.3:c.726+3534C>T
(NME7)
|
XP_005245163.1:n.726+3534C>T
|
|
NM_013330.5:c.1098+3534C>T
(NME7)
MANE Select
|
NP_037462.1:n.1098+3534C>T
|
|
NM_197972.3:c.990+3534C>T
(NME7)
|
NP_932076.1:n.990+3534C>T
|
|
NR_104229.2:n.1248+3534C>T
(NME7)
|
|
|