ENST00000305632.11:c.635T>A
MANE Select
|
ENSP00000307260.4:p.Val212Asp
|
|
ENST00000305632.9:c.635T>A
|
ENSP00000307260.4:p.Val212Asp
|
|
ENST00000417008.5:c.*372T>A
|
ENSP00000407503.1:n.*372T>A
|
|
ENST00000424598.5:c.*552T>A
|
ENSP00000398195.1:n.*552T>A
|
|
ENST00000426966.5:c.*568T>A
|
ENSP00000410737.1:n.*568T>A
|
|
ENST00000432538.5:c.527T>A
|
ENSP00000413979.1:p.Val176Asp
|
|
ENST00000433464.5:c.*244T>A
|
ENSP00000404242.1:n.*244T>A
|
|
ENST00000435792.5:c.*761T>A
|
ENSP00000408255.1:n.*761T>A
|
|
ENST00000437521.5:c.*568T>A
|
ENSP00000400569.1:n.*568T>A
|
|
ENST00000450285.5:c.*81T>A
|
ENSP00000409820.1:n.*81T>A
|
|
ENST00000452475.5:n.720T>A
|
|
|
ENST00000459913.5:n.802T>A
|
|
|
ENST00000495885.1:n.399T>A
|
|
|
ENST00000610724.4:c.635T>A
|
ENSP00000484750.1:p.Val212Asp
|
|
NM_012453.2:c.635T>A
|
NP_036585.1:p.Val212Asp
|
|
XM_006715923.2:c.536T>A
|
XP_006715986.1:p.Val179Asp
|
|
XM_011516026.1:c.527T>A
|
XP_011514328.1:p.Val176Asp
|
|
XM_011516027.1:c.140T>A
|
XP_011514329.1:p.Val47Asp
|
|
NM_001362660.1:c.536T>A
|
NP_001349589.1:p.Val179Asp
|
|
NM_001362661.1:c.140T>A
|
NP_001349590.1:p.Val47Asp
|
|
NM_001362662.1:c.140T>A
|
NP_001349591.1:p.Val47Asp
|
|
NM_001362663.1:c.140T>A
|
NP_001349592.1:p.Val47Asp
|
|
NM_012453.3:c.635T>A
|
NP_036585.1:p.Val212Asp
|
|
XM_006715923.4:c.536T>A
|
XP_006715986.1:p.Val179Asp
|
|
XM_024446709.1:c.536T>A
|
XP_024302477.1:p.Val179Asp
|
|
XM_024446712.1:c.140T>A
|
XP_024302480.1:p.Val47Asp
|
|
XR_001744627.2:n.691T>A
|
|
|
NM_001362660.2:c.536T>A
|
NP_001349589.1:p.Val179Asp
|
|
NM_001362661.2:c.140T>A
|
NP_001349590.1:p.Val47Asp
|
|
NM_001362662.2:c.140T>A
|
NP_001349591.1:p.Val47Asp
|
|
NM_001362663.2:c.140T>A
|
NP_001349592.1:p.Val47Asp
|
|
NM_012453.4:c.635T>A
MANE Select
|
NP_036585.1:p.Val212Asp
|
|