ENST00000367698.4:c.1225G>C
MANE Select
|
ENSP00000356671.3:p.Glu409Gln
|
|
ENST00000367698.3:c.1225G>C
|
ENSP00000356671.3:p.Glu409Gln
|
|
ENST00000617423.4:c.610G>C
|
ENSP00000478688.1:p.Glu204Gln
|
|
NM_000488.3:c.1225G>C , LRG_577t1:c.1225G>C
|
NP_000479.1:p.Glu409Gln
|
|
XM_005245198.2:c.1081G>C
|
XP_005245255.1:p.Glu361Gln
|
|
NM_001365052.1:c.1081G>C
|
NP_001351981.1:p.Glu361Gln
|
|
NM_000488.4:c.1225G>C
MANE Select
|
NP_000479.1:p.Glu409Gln
|
|
NM_001365052.2:c.1081G>C
|
NP_001351981.1:p.Glu361Gln
|
|
NM_001386302.1:c.1348G>C
|
NP_001373231.1:p.Glu450Gln
|
|
NM_001386303.1:c.1306G>C
|
NP_001373232.1:p.Glu436Gln
|
|
NM_001386304.1:c.1204G>C
|
NP_001373233.1:p.Glu402Gln
|
|
NM_001386305.1:c.1168G>C
|
NP_001373234.1:p.Glu390Gln
|
|
NM_001386306.1:c.1009G>C
|
NP_001373235.1:p.Glu337Gln
|
|