ENST00000367698.4:c.954C>A
MANE Select
|
ENSP00000356671.3:p.Pro318=
|
|
ENST00000367698.3:c.954C>A
|
ENSP00000356671.3:p.Pro318=
|
|
ENST00000487183.1:n.605C>A
|
|
|
ENST00000617423.4:c.559+2113C>A
|
ENSP00000478688.1:n.559+2113C>A
|
|
NM_000488.3:c.954C>A , LRG_577t1:c.954C>A
|
NP_000479.1:p.Pro318=
|
|
XM_005245198.2:c.810C>A
|
XP_005245255.1:p.Pro270=
|
|
NM_001365052.1:c.810C>A
|
NP_001351981.1:p.Pro270=
|
|
NM_000488.4:c.954C>A
MANE Select
|
NP_000479.1:p.Pro318=
|
|
NM_001365052.2:c.810C>A
|
NP_001351981.1:p.Pro270=
|
|
NM_001386302.1:c.1077C>A
|
NP_001373231.1:p.Pro359=
|
|
NM_001386303.1:c.1035C>A
|
NP_001373232.1:p.Pro345=
|
|
NM_001386304.1:c.933C>A
|
NP_001373233.1:p.Pro311=
|
|
NM_001386305.1:c.897C>A
|
NP_001373234.1:p.Pro299=
|
|
NM_001386306.1:c.738C>A
|
NP_001373235.1:p.Pro246=
|
|