|
ENST00000367698.4:c.843A>T
MANE Select
|
ENSP00000356671.3:p.Ala281=
|
|
|
ENST00000367698.3:c.843A>T
|
ENSP00000356671.3:p.Ala281=
|
|
|
ENST00000487183.1:n.494A>T
|
|
|
|
ENST00000617423.4:c.559+2002A>T
|
ENSP00000478688.1:n.559+2002A>T
|
|
|
NM_000488.3:c.843A>T , LRG_577t1:c.843A>T
|
NP_000479.1:p.Ala281=
|
|
|
XM_005245198.2:c.699A>T
|
XP_005245255.1:p.Ala233=
|
|
|
NM_001365052.1:c.699A>T
|
NP_001351981.1:p.Ala233=
|
|
|
NM_000488.4:c.843A>T
MANE Select
|
NP_000479.1:p.Ala281=
|
|
|
NM_001365052.2:c.699A>T
|
NP_001351981.1:p.Ala233=
|
|
|
NM_001386302.1:c.966A>T
|
NP_001373231.1:p.Ala322=
|
|
|
NM_001386303.1:c.924A>T
|
NP_001373232.1:p.Ala308=
|
|
|
NM_001386304.1:c.822A>T
|
NP_001373233.1:p.Ala274=
|
|
|
NM_001386305.1:c.786A>T
|
NP_001373234.1:p.Ala262=
|
|
|
NM_001386306.1:c.627A>T
|
NP_001373235.1:p.Ala209=
|
|
