ENST00000433473.8:c.855A>T
|
ENSP00000394863.4:p.Glu285Asp
|
|
ENST00000439754.6:c.786A>T
|
ENSP00000403207.2:p.Glu262Asp
|
|
ENST00000449045.7:c.549A>T
|
ENSP00000392293.2:p.Glu183Asp
|
|
ENST00000530076.6:c.201A>T
|
ENSP00000434007.1:p.Glu67Asp
|
|
ENST00000530704.6:c.*481A>T
|
ENSP00000431655.1:n.*481A>T
|
|
ENST00000641083.1:c.948A>T
|
|
|
ENST00000641236.1:n.1095A>T
|
|
|
ENST00000641319.1:c.*68A>T
|
ENSP00000493128.1:n.*68A>T
|
|
ENST00000641381.1:c.280A>T
|
|
|
ENST00000641471.1:c.945A>T
|
ENSP00000493146.1:p.Glu315Asp
|
|
ENST00000641691.1:c.*710A>T
|
ENSP00000492910.1:n.*710A>T
|
|
ENST00000641924.1:c.*287A>T
|
ENSP00000493063.1:n.*287A>T
|
|
ENST00000642050.2:c.858A>T
MANE Select
|
ENSP00000493153.1:p.Glu286Asp
|
|
ENST00000372775.2:n.255A>T
|
|
|
ENST00000433473.7:c.858A>T
|
ENSP00000394863.3:p.Glu286Asp
|
|
ENST00000439754.5:c.471A>T
|
ENSP00000403207.1:p.Glu157Asp
|
|
ENST00000449045.6:c.549A>T
|
ENSP00000392293.2:p.Glu183Asp
|
|
ENST00000529905.5:c.858A>T
|
ENSP00000432053.1:p.Glu286Asp
|
|
ENST00000530076.5:c.201A>T
|
ENSP00000434007.1:p.Glu67Asp
|
|
ENST00000530704.5:c.*481A>T
|
ENSP00000431655.1:n.*481A>T
|
|
NM_000310.3:c.858A>T , LRG_690t1:c.858A>T
|
NP_000301.1:p.Glu286Asp
|
|
NM_001142604.1:c.549A>T
|
NP_001136076.1:p.Glu183Asp
|
|
XM_005271008.1:c.786A>T
|
XP_005271065.1:p.Glu262Asp
|
|
NM_001363695.1:c.786A>T
|
NP_001350624.1:p.Glu262Asp
|
|
NM_000310.4:c.858A>T
MANE Select
|
NP_000301.1:p.Glu286Asp
|
|
NM_001142604.2:c.549A>T
|
NP_001136076.1:p.Glu183Asp
|
|
NM_001363695.2:c.786A>T
|
NP_001350624.1:p.Glu262Asp
|
|