ENST00000247933.9:c.1527C>G
|
ENSP00000247933.4:p.Asp509Glu
|
|
ENST00000514224.2:c.1527C>G
MANE Select
|
ENSP00000425081.2:p.Asp509Glu
|
|
ENST00000652070.1:n.1583C>G
|
|
|
ENST00000247933.8:c.1527C>G
|
ENSP00000247933.4:p.Asp509Glu
|
|
ENST00000502829.1:n.516C>G
|
|
|
ENST00000514224.1:c.1131C>G
|
ENSP00000425081.1:p.Asp377Glu
|
|
ENST00000514698.5:n.1634C>G
|
|
|
NM_000203.4:c.1527C>G
|
NP_000194.2:p.Asp509Glu
|
|
NR_110313.1:n.1615C>G
|
|
|
XM_006713882.2:c.1131C>G
|
XP_006713945.1:p.Asp377Glu
|
|
XM_011513459.1:c.1593C>G
|
XP_011511761.1:p.Asp531Glu
|
|
XM_011513460.1:c.1386C>G
|
XP_011511762.1:p.Asp462Glu
|
|
XM_011513461.1:c.1320C>G
|
XP_011511763.1:p.Asp440Glu
|
|
XM_011513462.1:c.1239C>G
|
XP_011511764.1:p.Asp413Glu
|
|
XM_011513463.1:c.1239C>G
|
XP_011511765.1:p.Asp413Glu
|
|
XR_924947.1:n.1783C>G
|
|
|
NM_000203.5:c.1527C>G
MANE Select
|
NP_000194.2:p.Asp509Glu
|
|
NM_001363576.1:c.1131C>G
|
NP_001350505.1:p.Asp377Glu
|
|
XM_011513461.2:c.1320C>G
|
XP_011511763.1:p.Asp440Glu
|
|
XM_017008163.1:c.567C>G
|
XP_016863652.1:p.Asp189Glu
|
|