ENST00000433473.8:c.874T=
|
ENSP00000394863.4:p.Ser292=
|
|
ENST00000439754.6:c.805T=
|
ENSP00000403207.2:p.Ser269=
|
|
ENST00000449045.7:c.568T=
|
ENSP00000392293.2:p.Ser190=
|
|
ENST00000530076.6:c.220T=
|
ENSP00000434007.1:p.Ser74=
|
|
ENST00000530704.6:c.*500T=
|
ENSP00000431655.1:n.*500T=
|
|
ENST00000641083.1:c.967T=
|
|
|
ENST00000641236.1:n.1114T=
|
|
|
ENST00000641319.1:c.*87T=
|
ENSP00000493128.1:n.*87T=
|
|
ENST00000641381.1:c.299T=
|
|
|
ENST00000641471.1:c.964T=
|
ENSP00000493146.1:p.Ser322=
|
|
ENST00000641691.1:c.*729T=
|
ENSP00000492910.1:n.*729T=
|
|
ENST00000641924.1:c.*306T=
|
ENSP00000493063.1:n.*306T=
|
|
ENST00000642050.2:c.877T=
MANE Select
|
ENSP00000493153.1:p.Ser293=
|
|
ENST00000372775.2:n.274T=
|
|
|
ENST00000433473.7:c.877T=
|
ENSP00000394863.3:p.Ser293=
|
|
ENST00000439754.5:c.490T=
|
ENSP00000403207.1:p.Ser164=
|
|
ENST00000449045.6:c.568T=
|
ENSP00000392293.2:p.Ser190=
|
|
ENST00000529905.5:c.877T=
|
ENSP00000432053.1:p.Ser293=
|
|
ENST00000530076.5:c.220T=
|
ENSP00000434007.1:p.Ser74=
|
|
ENST00000530704.5:c.*500T=
|
ENSP00000431655.1:n.*500T=
|
|
NM_000310.3:c.877T= , LRG_690t1:c.877T=
|
NP_000301.1:p.Ser293=
|
|
NM_001142604.1:c.568T=
|
NP_001136076.1:p.Ser190=
|
|
XM_005271008.1:c.805T=
|
XP_005271065.1:p.Ser269=
|
|
NM_001363695.1:c.805T=
|
NP_001350624.1:p.Ser269=
|
|
NM_000310.4:c.877T=
MANE Select
|
NP_000301.1:p.Ser293=
|
|
NM_001142604.2:c.568T=
|
NP_001136076.1:p.Ser190=
|
|
NM_001363695.2:c.805T=
|
NP_001350624.1:p.Ser269=
|
|