|
ENST00000367698.4:c.763-2A>C
MANE Select
|
ENSP00000356671.3:n.763-2A>C
|
|
|
ENST00000367698.3:c.763-2A>C
|
ENSP00000356671.3:n.763-2A>C
|
|
|
ENST00000487183.1:n.414-2A>C
|
|
|
|
ENST00000617423.4:c.559+1920A>C
|
ENSP00000478688.1:n.559+1920A>C
|
|
|
NM_000488.3:c.763-2A>C , LRG_577t1:c.763-2A>C
|
NP_000479.1:n.763-2A>C
|
|
|
XM_005245198.2:c.619-2A>C
|
XP_005245255.1:n.619-2A>C
|
|
|
NM_001365052.1:c.619-2A>C
|
NP_001351981.1:n.619-2A>C
|
|
|
NM_000488.4:c.763-2A>C
MANE Select
|
NP_000479.1:n.763-2A>C
|
|
|
NM_001365052.2:c.619-2A>C
|
NP_001351981.1:n.619-2A>C
|
|
|
NM_001386302.1:c.886-2A>C
|
NP_001373231.1:n.886-2A>C
|
|
|
NM_001386303.1:c.844-2A>C
|
NP_001373232.1:n.844-2A>C
|
|
|
NM_001386304.1:c.742-2A>C
|
NP_001373233.1:n.742-2A>C
|
|
|
NM_001386305.1:c.763-59A>C
|
NP_001373234.1:n.763-59A>C
|
|
|
NM_001386306.1:c.547-2A>C
|
NP_001373235.1:n.547-2A>C
|
|
