ENST00000367698.4:c.1112G>A
MANE Select
|
ENSP00000356671.3:p.Gly371Asp
|
|
ENST00000367698.3:c.1112G>A
|
ENSP00000356671.3:p.Gly371Asp
|
|
ENST00000617423.4:c.560-2100G>A
|
ENSP00000478688.1:n.560-2100G>A
|
|
NM_000488.3:c.1112G>A , LRG_577t1:c.1112G>A
|
NP_000479.1:p.Gly371Asp
|
|
XM_005245198.2:c.968G>A
|
XP_005245255.1:p.Gly323Asp
|
|
NM_001365052.1:c.968G>A
|
NP_001351981.1:p.Gly323Asp
|
|
NM_000488.4:c.1112G>A
MANE Select
|
NP_000479.1:p.Gly371Asp
|
|
NM_001365052.2:c.968G>A
|
NP_001351981.1:p.Gly323Asp
|
|
NM_001386302.1:c.1235G>A
|
NP_001373231.1:p.Gly412Asp
|
|
NM_001386303.1:c.1193G>A
|
NP_001373232.1:p.Gly398Asp
|
|
NM_001386304.1:c.1091G>A
|
NP_001373233.1:p.Gly364Asp
|
|
NM_001386305.1:c.1055G>A
|
NP_001373234.1:p.Gly352Asp
|
|
NM_001386306.1:c.896G>A
|
NP_001373235.1:p.Gly299Asp
|
|