ENST00000700061.1:c.1064C>A
|
|
|
ENST00000700062.1:c.1064C>A
|
|
|
ENST00000700065.1:n.2980C>A
|
|
|
ENST00000281513.10:c.2967C>A
MANE Select
|
ENSP00000281513.5:p.Asp989Glu
|
|
ENST00000281513.9:c.2967C>A
|
ENSP00000281513.5:p.Asp989Glu
|
|
ENST00000429842.1:c.259C>A
|
|
|
ENST00000441755.5:c.108C>A
|
ENSP00000396501.1:p.Asp36Glu
|
|
ENST00000442506.5:c.110C>A
|
|
|
NM_015909.3:c.2967C>A
|
NP_056993.2:p.Asp989Glu
|
|
NR_052013.2:n.3011C>A
|
|
|
XM_011510357.1:c.2838C>A
|
XP_011508659.1:p.Asp946Glu
|
|
XM_011510358.1:c.2967C>A
|
XP_011508660.1:p.Asp989Glu
|
|
XM_011510359.1:c.2328C>A
|
XP_011508661.1:p.Asp776Glu
|
|
XM_011510360.1:c.768C>A
|
XP_011508662.1:p.Asp256Glu
|
|
XM_011510361.1:c.759C>A
|
XP_011508663.1:p.Asp253Glu
|
|
XM_011510357.2:c.2838C>A
|
XP_011508659.1:p.Asp946Glu
|
|
XM_011510358.2:c.2967C>A
|
XP_011508660.1:p.Asp989Glu
|
|
XM_011510360.2:c.768C>A
|
XP_011508662.1:p.Asp256Glu
|
|
XM_011510361.2:c.759C>A
|
XP_011508663.1:p.Asp253Glu
|
|
XM_017004317.1:c.2967C>A
|
XP_016859806.1:p.Asp989Glu
|
|
XM_024452961.1:c.2328C>A
|
XP_024308729.1:p.Asp776Glu
|
|
NM_015909.4:c.2967C>A
MANE Select
|
NP_056993.2:p.Asp989Glu
|
|
NR_052013.3:n.2997C>A
|
|
|