|
ENST00000614091.5:c.237G>T
|
ENSP00000482097.2:p.Glu79Asp
|
|
|
ENST00000623113.3:c.237G>T
|
ENSP00000485413.2:p.Glu79Asp
|
|
|
ENST00000323670.14:c.237G>T
MANE Select
|
ENSP00000313332.9:p.Glu79Asp
|
|
|
ENST00000323670.13:c.237G>T
|
ENSP00000313332.8:p.Glu79Asp
|
|
|
ENST00000342680.5:c.*151G>T
|
ENSP00000345497.5:n.*151G>T
|
|
|
ENST00000392275.1:n.628G>T
|
|
|
|
ENST00000392276.1:c.45G>T
|
ENSP00000376102.1:p.Glu15Asp
|
|
|
ENST00000392278.2:c.270G>T
|
ENSP00000376103.2:p.Glu90Asp
|
|
|
ENST00000591243.1:c.237G>T
|
ENSP00000467516.1:p.Glu79Asp
|
|
|
ENST00000592153.5:c.237G>T
|
ENSP00000467117.1:p.Glu79Asp
|
|
|
ENST00000614091.4:c.237G>T
|
ENSP00000482097.1:p.Glu79Asp
|
|
|
ENST00000623113.1:c.45G>T
|
ENSP00000485413.1:p.Glu15Asp
|
|
|
NM_001031726.3:c.270G>T
|
NP_001026896.2:p.Glu90Asp
|
|
|
NM_001256046.1:c.237G>T
|
NP_001242975.1:p.Glu79Asp
|
|
|
NM_001256047.1:c.237G>T
|
NP_001242976.1:p.Glu79Asp
|
|
|
NM_001282929.1:c.45G>T
|
NP_001269858.1:p.Glu15Asp
|
|
|
NM_001282930.1:c.45G>T
|
NP_001269859.1:p.Glu15Asp
|
|
|
NM_001282931.1:c.45G>T
|
NP_001269860.1:p.Glu15Asp
|
|
|
NM_031448.4:c.237G>T
|
NP_113636.2:p.Glu79Asp
|
|
|
XM_024451734.1:c.399G>T
|
XP_024307502.1:p.Glu133Asp
|
|
|
XM_024451735.1:c.237G>T
|
XP_024307503.1:p.Glu79Asp
|
|
|
XM_024451736.1:c.237G>T
|
XP_024307504.1:p.Glu79Asp
|
|
|
XM_024451737.1:c.237G>T
|
XP_024307505.1:p.Glu79Asp
|
|
|
XM_024451738.1:c.237G>T
|
XP_024307506.1:p.Glu79Asp
|
|
|
NM_001256046.2:c.237G>T
|
NP_001242975.1:p.Glu79Asp
|
|
|
NM_001282930.2:c.45G>T
|
NP_001269859.1:p.Glu15Asp
|
|
|
NM_001282931.2:c.45G>T
|
NP_001269860.1:p.Glu15Asp
|
|
|
NM_031448.6:c.237G>T
MANE Select
|
NP_113636.2:p.Glu79Asp
|
|
|
NM_001031726.4:c.237G>T
|
NP_001026896.3:p.Glu79Asp
|
|
|
NM_001256046.3:c.237G>T
|
NP_001242975.1:p.Glu79Asp
|
|
|
NM_001256047.2:c.237G>T
|
NP_001242976.1:p.Glu79Asp
|
|
|
NM_001282930.3:c.45G>T
|
NP_001269859.1:p.Glu15Asp
|
|
|
NM_001282931.3:c.45G>T
|
NP_001269860.1:p.Glu15Asp
|
|
