ENST00000257904.11:c.168G>C
MANE Select
|
ENSP00000257904.5:p.Glu56Asp
|
|
ENST00000257904.10:c.168G>C
|
ENSP00000257904.5:p.Glu56Asp
|
|
ENST00000312990.10:c.168G>C
|
ENSP00000316889.6:p.Glu56Asp
|
|
ENST00000546489.5:c.-4-208G>C
|
ENSP00000447779.1:n.-4-208G>C
|
|
ENST00000547281.5:c.-55G>C
|
ENSP00000447274.1:n.-55G>C
|
|
ENST00000549606.5:c.-158+625G>C
|
ENSP00000447005.1:n.-158+625G>C
|
|
ENST00000550419.5:c.168G>C
|
ENSP00000448098.1:p.Glu56Asp
|
|
ENST00000551706.1:n.377G>C
|
|
|
ENST00000551800.5:c.-55G>C
|
ENSP00000449391.1:n.-55G>C
|
|
ENST00000551888.5:n.346G>C
|
|
|
ENST00000552254.5:c.168G>C
|
ENSP00000449179.1:p.Glu56Asp
|
|
ENST00000552388.1:c.168G>C
|
ENSP00000448963.1:p.Glu56Asp
|
|
ENST00000552862.1:c.168G>C
|
ENSP00000446763.1:p.Glu56Asp
|
|
ENST00000553237.5:c.168G>C
|
ENSP00000448885.1:p.Glu56Asp
|
|
NM_000075.3:c.168G>C
|
NP_000066.1:p.Glu56Asp
|
|
NM_000075.4:c.168G>C
MANE Select
|
NP_000066.1:p.Glu56Asp
|
|