ENST00000348974.5:c.681A>C
|
ENSP00000330021.7:p.Glu227Asp
|
|
ENST00000394236.9:c.681A>C
MANE Select
|
ENSP00000377783.3:p.Glu227Asp
|
|
ENST00000407433.6:c.636A>C
|
ENSP00000385794.2:p.Glu212Asp
|
|
ENST00000647936.1:c.681A>C
|
ENSP00000496822.1:p.Glu227Asp
|
|
ENST00000648381.1:n.849A>C
|
|
|
ENST00000648853.1:c.639A>C
|
ENSP00000497262.1:p.Glu213Asp
|
|
ENST00000649103.1:c.780A>C
|
ENSP00000497962.1:n.780A>C
|
|
ENST00000650591.1:c.777A>C
|
ENSP00000497376.1:p.Glu259Asp
|
|
ENST00000394236.7:c.681A>C
|
ENSP00000377783.3:p.Glu227Asp
|
|
ENST00000407433.5:c.288A>C
|
ENSP00000385794.1:p.Glu96Asp
|
|
NM_000313.3:c.681A>C , LRG_572t1:c.681A>C
|
NP_000304.2:p.Glu227Asp
|
|
NM_001314077.1:c.777A>C , LRG_572t2:c.777A>C
|
NP_001301006.1:p.Glu259Asp
|
|
NM_000313.4:c.681A>C
MANE Select
|
NP_000304.2:p.Glu227Asp
|
|
NM_001314077.2:c.777A>C
|
NP_001301006.1:p.Glu259Asp
|
|