ENST00000367698.4:c.792G>C
MANE Select
|
ENSP00000356671.3:p.Glu264Asp
|
|
ENST00000367698.3:c.792G>C
|
ENSP00000356671.3:p.Glu264Asp
|
|
ENST00000487183.1:n.443G>C
|
|
|
ENST00000617423.4:c.559+1951G>C
|
ENSP00000478688.1:n.559+1951G>C
|
|
NM_000488.3:c.792G>C , LRG_577t1:c.792G>C
|
NP_000479.1:p.Glu264Asp
|
|
XM_005245198.2:c.648G>C
|
XP_005245255.1:p.Glu216Asp
|
|
NM_001365052.1:c.648G>C
|
NP_001351981.1:p.Glu216Asp
|
|
NM_000488.4:c.792G>C
MANE Select
|
NP_000479.1:p.Glu264Asp
|
|
NM_001365052.2:c.648G>C
|
NP_001351981.1:p.Glu216Asp
|
|
NM_001386302.1:c.915G>C
|
NP_001373231.1:p.Glu305Asp
|
|
NM_001386303.1:c.873G>C
|
NP_001373232.1:p.Glu291Asp
|
|
NM_001386304.1:c.771G>C
|
NP_001373233.1:p.Glu257Asp
|
|
NM_001386305.1:c.763-28G>C
|
NP_001373234.1:n.763-28G>C
|
|
NM_001386306.1:c.576G>C
|
NP_001373235.1:p.Glu192Asp
|
|