|
ENST00000367698.4:c.926A>T
MANE Select
|
ENSP00000356671.3:p.Asp309Val
|
|
|
ENST00000367698.3:c.926A>T
|
ENSP00000356671.3:p.Asp309Val
|
|
|
ENST00000487183.1:n.577A>T
|
|
|
|
ENST00000617423.4:c.559+2085A>T
|
ENSP00000478688.1:n.559+2085A>T
|
|
|
NM_000488.3:c.926A>T , LRG_577t1:c.926A>T
|
NP_000479.1:p.Asp309Val
|
|
|
XM_005245198.2:c.782A>T
|
XP_005245255.1:p.Asp261Val
|
|
|
NM_001365052.1:c.782A>T
|
NP_001351981.1:p.Asp261Val
|
|
|
NM_000488.4:c.926A>T
MANE Select
|
NP_000479.1:p.Asp309Val
|
|
|
NM_001365052.2:c.782A>T
|
NP_001351981.1:p.Asp261Val
|
|
|
NM_001386302.1:c.1049A>T
|
NP_001373231.1:p.Asp350Val
|
|
|
NM_001386303.1:c.1007A>T
|
NP_001373232.1:p.Asp336Val
|
|
|
NM_001386304.1:c.905A>T
|
NP_001373233.1:p.Asp302Val
|
|
|
NM_001386305.1:c.869A>T
|
NP_001373234.1:p.Asp290Val
|
|
|
NM_001386306.1:c.710A>T
|
NP_001373235.1:p.Asp237Val
|
|
