ENST00000367698.4:c.1074G>C
MANE Select
|
ENSP00000356671.3:p.Glu358Asp
|
|
ENST00000367698.3:c.1074G>C
|
ENSP00000356671.3:p.Glu358Asp
|
|
ENST00000617423.4:c.560-2138G>C
|
ENSP00000478688.1:n.560-2138G>C
|
|
NM_000488.3:c.1074G>C , LRG_577t1:c.1074G>C
|
NP_000479.1:p.Glu358Asp
|
|
XM_005245198.2:c.930G>C
|
XP_005245255.1:p.Glu310Asp
|
|
NM_001365052.1:c.930G>C
|
NP_001351981.1:p.Glu310Asp
|
|
NM_000488.4:c.1074G>C
MANE Select
|
NP_000479.1:p.Glu358Asp
|
|
NM_001365052.2:c.930G>C
|
NP_001351981.1:p.Glu310Asp
|
|
NM_001386302.1:c.1197G>C
|
NP_001373231.1:p.Glu399Asp
|
|
NM_001386303.1:c.1155G>C
|
NP_001373232.1:p.Glu385Asp
|
|
NM_001386304.1:c.1053G>C
|
NP_001373233.1:p.Glu351Asp
|
|
NM_001386305.1:c.1017G>C
|
NP_001373234.1:p.Glu339Asp
|
|
NM_001386306.1:c.858G>C
|
NP_001373235.1:p.Glu286Asp
|
|