ENST00000272602.7:c.450G>T
MANE Select
|
ENSP00000272602.2:p.Glu150Asp
|
|
ENST00000272602.6:c.450G>T
|
ENSP00000272602.2:p.Glu150Asp
|
|
ENST00000393503.2:n.455G>T
|
|
|
ENST00000393504.5:c.450G>T
|
ENSP00000377140.1:p.Glu150Asp
|
|
ENST00000409937.1:c.462G>T
|
ENSP00000386761.1:p.Glu154Asp
|
|
ENST00000436404.6:c.396G>T
|
ENSP00000410070.2:p.Arg132Ser
|
|
NM_001079878.1:c.396G>T
|
NP_001073347.1:p.Arg132Ser
|
|
NM_001298.2:c.450G>T
|
NP_001289.1:p.Glu150Asp
|
|
XM_006712243.2:c.561G>T
|
XP_006712306.1:p.Arg187Ser
|
|
XM_011510554.1:c.615G>T
|
XP_011508856.1:p.Glu205Asp
|
|
XM_011510554.2:c.615G>T
|
XP_011508856.1:p.Glu205Asp
|
|
NM_001079878.2:c.396G>T
|
NP_001073347.1:p.Arg132Ser
|
|
NM_001298.3:c.450G>T
MANE Select
|
NP_001289.1:p.Glu150Asp
|
|