ENST00000402696.9:c.1773G>T
MANE Select
|
ENSP00000385834.3:p.Glu591Asp
|
|
ENST00000402696.7:c.1773G>T
|
ENSP00000385834.3:p.Glu591Asp
|
|
ENST00000461695.1:c.504G>T
|
|
|
ENST00000467842.1:n.2767G>T
|
|
|
NM_001063.3:c.1773G>T
|
NP_001054.1:p.Glu591Asp
|
|
XM_011513100.1:c.1773G>T
|
XP_011511402.1:p.Glu591Asp
|
|
NM_001354703.1:c.1641G>T
|
NP_001341632.1:p.Glu547Asp
|
|
NM_001354704.1:c.1392G>T
|
NP_001341633.1:p.Glu464Asp
|
|
NM_001063.4:c.1773G>T
MANE Select
|
NP_001054.2:p.Glu591Asp
|
|
NM_001354703.2:c.1641G>T
|
NP_001341632.2:p.Glu547Asp
|
|
NM_001354704.2:c.1392G>T
|
NP_001341633.2:p.Glu464Asp
|
|