ENST00000247933.9:c.1713A>T
|
ENSP00000247933.4:p.Glu571Asp
|
|
ENST00000514224.2:c.1713A>T
MANE Select
|
ENSP00000425081.2:p.Glu571Asp
|
|
ENST00000652070.1:n.1769A>T
|
|
|
ENST00000247933.8:c.1713A>T
|
ENSP00000247933.4:p.Glu571Asp
|
|
ENST00000514224.1:c.1317A>T
|
ENSP00000425081.1:p.Glu439Asp
|
|
ENST00000514417.1:n.105A>T
|
|
|
ENST00000514698.5:n.1820A>T
|
|
|
NM_000203.4:c.1713A>T
|
NP_000194.2:p.Glu571Asp
|
|
NR_110313.1:n.1801A>T
|
|
|
XM_006713882.2:c.1317A>T
|
XP_006713945.1:p.Glu439Asp
|
|
XM_011513459.1:c.1779A>T
|
XP_011511761.1:p.Glu593Asp
|
|
XM_011513460.1:c.1572A>T
|
XP_011511762.1:p.Glu524Asp
|
|
XM_011513461.1:c.1506A>T
|
XP_011511763.1:p.Glu502Asp
|
|
XM_011513462.1:c.1425A>T
|
XP_011511764.1:p.Glu475Asp
|
|
XM_011513463.1:c.1425A>T
|
XP_011511765.1:p.Glu475Asp
|
|
XR_924947.1:n.1969A>T
|
|
|
NM_000203.5:c.1713A>T
MANE Select
|
NP_000194.2:p.Glu571Asp
|
|
NM_001363576.1:c.1317A>T
|
NP_001350505.1:p.Glu439Asp
|
|
XM_011513461.2:c.1506A>T
|
XP_011511763.1:p.Glu502Asp
|
|
XM_017008163.1:c.753A>T
|
XP_016863652.1:p.Glu251Asp
|
|