ENST00000332981.11:c.1059C>A
MANE Select
|
ENSP00000329127.5:p.Asp353Glu
|
|
ENST00000332981.10:c.1059C>A
|
ENSP00000329127.5:p.Asp353Glu
|
|
ENST00000332981.9:c.1059C>A
|
ENSP00000329127.5:p.Asp353Glu
|
|
ENST00000553889.5:n.360C>A
|
|
|
ENST00000555082.5:c.576C>A
|
ENSP00000450981.1:p.Asp192Glu
|
|
ENST00000555185.5:c.-18-28228C>A
|
ENSP00000451871.1:n.-18-28228C>A
|
|
ENST00000557559.1:n.339C>A
|
|
|
ENST00000557585.5:c.576C>A
|
ENSP00000451930.1:p.Asp192Glu
|
|
NM_006255.4:c.1059C>A
|
NP_006246.2:p.Asp353Glu
|
|
XM_011536954.1:c.822C>A
|
XP_011535256.1:p.Asp274Glu
|
|
XM_011536955.1:c.819C>A
|
XP_011535257.1:p.Asp273Glu
|
|
XM_011536956.1:c.1059C>A
|
XP_011535258.1:p.Asp353Glu
|
|
XM_011536957.1:c.1059C>A
|
XP_011535259.1:p.Asp353Glu
|
|
XM_011536954.3:c.822C>A
|
XP_011535256.1:p.Asp274Glu
|
|
XM_017021458.1:c.576C>A
|
XP_016876947.1:p.Asp192Glu
|
|
XM_017021459.1:c.1059C>A
|
XP_016876948.1:p.Asp353Glu
|
|
XM_024449661.1:c.576C>A
|
XP_024305429.1:p.Asp192Glu
|
|
XM_024449662.1:c.576C>A
|
XP_024305430.1:p.Asp192Glu
|
|
NM_006255.5:c.1059C>A
MANE Select
|
NP_006246.2:p.Asp353Glu
|
|