ENST00000403733.8:c.3344A>G
MANE Select
|
ENSP00000384222.3:p.Asp1115Gly
|
|
ENST00000403733.7:c.3344A>G
|
ENSP00000384222.3:p.Asp1115Gly
|
|
ENST00000427431.5:c.*2736A>G
|
ENSP00000393342.1:n.*2736A>G
|
|
ENST00000438543.5:c.*1140A>G
|
ENSP00000413521.1:n.*1140A>G
|
|
ENST00000448232.6:c.3416A>G
|
ENSP00000398577.2:p.Asp1139Gly
|
|
ENST00000504005.5:c.2390A>G
|
ENSP00000427569.1:p.Asp797Gly
|
|
ENST00000508747.1:c.728A>G
|
ENSP00000420835.1:p.Asp243Gly
|
|
ENST00000513834.5:c.3197A>G
|
ENSP00000425054.1:p.Asp1066Gly
|
|
NM_024949.5:c.3344A>G
|
NP_079225.5:p.Asp1115Gly
|
|
XM_011532269.1:c.3416A>G
|
XP_011530571.1:p.Asp1139Gly
|
|
XM_011532269.3:c.3416A>G
|
XP_011530571.1:p.Asp1139Gly
|
|
XM_024454225.1:c.3122A>G
|
XP_024309993.1:p.Asp1041Gly
|
|
NM_024949.6:c.3344A>G
MANE Select
|
NP_079225.5:p.Asp1115Gly
|
|