ENST00000367698.4:c.1121A>T
MANE Select
|
ENSP00000356671.3:p.Asp374Val
|
|
ENST00000367698.3:c.1121A>T
|
ENSP00000356671.3:p.Asp374Val
|
|
ENST00000617423.4:c.560-2091A>T
|
ENSP00000478688.1:n.560-2091A>T
|
|
NM_000488.3:c.1121A>T , LRG_577t1:c.1121A>T
|
NP_000479.1:p.Asp374Val
|
|
XM_005245198.2:c.977A>T
|
XP_005245255.1:p.Asp326Val
|
|
NM_001365052.1:c.977A>T
|
NP_001351981.1:p.Asp326Val
|
|
NM_000488.4:c.1121A>T
MANE Select
|
NP_000479.1:p.Asp374Val
|
|
NM_001365052.2:c.977A>T
|
NP_001351981.1:p.Asp326Val
|
|
NM_001386302.1:c.1244A>T
|
NP_001373231.1:p.Asp415Val
|
|
NM_001386303.1:c.1202A>T
|
NP_001373232.1:p.Asp401Val
|
|
NM_001386304.1:c.1100A>T
|
NP_001373233.1:p.Asp367Val
|
|
NM_001386305.1:c.1064A>T
|
NP_001373234.1:p.Asp355Val
|
|
NM_001386306.1:c.905A>T
|
NP_001373235.1:p.Asp302Val
|
|