ENST00000367698.4:c.1153+70A>T
MANE Select
|
ENSP00000356671.3:n.1153+70A>T
|
|
ENST00000367698.3:c.1153+70A>T
|
ENSP00000356671.3:n.1153+70A>T
|
|
ENST00000617423.4:c.560-1989A>T
|
ENSP00000478688.1:n.560-1989A>T
|
|
NM_000488.3:c.1153+70A>T , LRG_577t1:c.1153+70A>T
|
NP_000479.1:n.1153+70A>T
|
|
XM_005245198.2:c.1009+70A>T
|
XP_005245255.1:n.1009+70A>T
|
|
NM_001365052.1:c.1009+70A>T
|
NP_001351981.1:n.1009+70A>T
|
|
NM_000488.4:c.1153+70A>T
MANE Select
|
NP_000479.1:n.1153+70A>T
|
|
NM_001365052.2:c.1009+70A>T
|
NP_001351981.1:n.1009+70A>T
|
|
NM_001386302.1:c.1276+70A>T
|
NP_001373231.1:n.1276+70A>T
|
|
NM_001386303.1:c.1234+70A>T
|
NP_001373232.1:n.1234+70A>T
|
|
NM_001386304.1:c.1132+70A>T
|
NP_001373233.1:n.1132+70A>T
|
|
NM_001386305.1:c.1096+70A>T
|
NP_001373234.1:n.1096+70A>T
|
|
NM_001386306.1:c.937+70A>T
|
NP_001373235.1:n.937+70A>T
|
|