|
ENST00000367698.4:c.1219-34G=
MANE Select
|
ENSP00000356671.3:n.1219-34G=
|
|
|
ENST00000367698.3:c.1219-34G=
|
ENSP00000356671.3:n.1219-34G=
|
|
|
ENST00000617423.4:c.604-34G=
|
ENSP00000478688.1:n.604-34G=
|
|
|
NM_000488.3:c.1219-34G= , LRG_577t1:c.1219-34G=
|
NP_000479.1:n.1219-34G=
|
|
|
XM_005245198.2:c.1075-34G=
|
XP_005245255.1:n.1075-34G=
|
|
|
NM_001365052.1:c.1075-34G=
|
NP_001351981.1:n.1075-34G=
|
|
|
NM_000488.4:c.1219-34G=
MANE Select
|
NP_000479.1:n.1219-34G=
|
|
|
NM_001365052.2:c.1075-34G=
|
NP_001351981.1:n.1075-34G=
|
|
|
NM_001386302.1:c.1342-34G=
|
NP_001373231.1:n.1342-34G=
|
|
|
NM_001386303.1:c.1300-34G=
|
NP_001373232.1:n.1300-34G=
|
|
|
NM_001386304.1:c.1198-34G=
|
NP_001373233.1:n.1198-34G=
|
|
|
NM_001386305.1:c.1162-34G=
|
NP_001373234.1:n.1162-34G=
|
|
|
NM_001386306.1:c.1003-34G=
|
NP_001373235.1:n.1003-34G=
|
|
