ENST00000264499.9:c.618C>A
MANE Select
|
ENSP00000264499.4:p.Asp206Glu
|
|
ENST00000264499.8:c.618C>A
|
ENSP00000264499.4:p.Asp206Glu
|
|
ENST00000506636.1:c.618C>A
|
ENSP00000423626.1:p.Asp206Glu
|
|
NM_018190.3:c.618C>A
|
NP_060660.2:p.Asp206Glu
|
|
NM_176824.2:c.618C>A
|
NP_789794.1:p.Asp206Glu
|
|
XM_005263106.2:c.621C>A
|
XP_005263163.1:p.Asp207Glu
|
|
XM_011532079.1:c.666C>A
|
XP_011530381.1:p.Asp222Glu
|
|
XM_011532080.1:c.663C>A
|
XP_011530382.1:p.Asp221Glu
|
|
XM_011532081.1:c.666C>A
|
XP_011530383.1:p.Asp222Glu
|
|
XM_005263106.4:c.621C>A
|
XP_005263163.1:p.Asp207Glu
|
|
XM_011532079.3:c.666C>A
|
XP_011530381.1:p.Asp222Glu
|
|
XM_011532080.3:c.663C>A
|
XP_011530382.1:p.Asp221Glu
|
|
XM_011532081.3:c.666C>A
|
XP_011530383.1:p.Asp222Glu
|
|
XM_017008357.2:c.618C>A
|
XP_016863846.1:p.Asp206Glu
|
|
XM_017008358.2:c.621C>A
|
XP_016863847.1:p.Asp207Glu
|
|
NM_176824.3:c.618C>A
MANE Select
|
NP_789794.1:p.Asp206Glu
|
|
NM_018190.4:c.618C>A
|
NP_060660.2:p.Asp206Glu
|
|