ENST00000374479.4:c.1059A>T
MANE Select
|
ENSP00000363603.3:p.Glu353Asp
|
|
ENST00000374479.3:c.1059A>T
|
ENSP00000363603.3:p.Glu353Asp
|
|
NM_000147.4:c.1059A>T
|
NP_000138.2:p.Glu353Asp
|
|
XM_005245821.1:c.684A>T
|
XP_005245878.1:p.Glu228Asp
|
|
XM_011541167.1:c.426A>T
|
XP_011539469.1:p.Glu142Asp
|
|
XM_005245821.3:c.684A>T
|
XP_005245878.1:p.Glu228Asp
|
|
XM_011541167.3:c.426A>T
|
XP_011539469.1:p.Glu142Asp
|
|
XM_017000905.2:c.756A>T
|
XP_016856394.1:p.Glu252Asp
|
|
NM_000147.5:c.1059A>T
MANE Select
|
NP_000138.2:p.Glu353Asp
|
|
NR_174379.1:n.1237A>T
|
|
|
NR_174380.1:n.1286A>T
|
|
|
NR_174381.1:n.1125A>T
|
|
|
NR_174382.1:n.1522A>T
|
|
|