ENST00000682275.1:c.1152G>C
|
ENSP00000507852.1:p.Glu384Asp
|
|
ENST00000683395.1:c.1093G>C
|
|
|
ENST00000684087.1:c.1116G>C
|
ENSP00000506978.1:p.Glu372Asp
|
|
ENST00000506362.2:c.867G>C
|
ENSP00000424103.2:p.Glu289Asp
|
|
ENST00000673642.1:c.775G>C
|
ENSP00000501242.1:p.Glu259Gln
|
|
ENST00000673991.1:c.1152G>C
|
ENSP00000501033.1:p.Glu384Asp
|
|
ENST00000226760.5:c.1116G>C
MANE Select
|
ENSP00000226760.1:p.Glu372Asp
|
|
ENST00000503569.5:c.1116G>C
|
ENSP00000423337.1:p.Glu372Asp
|
|
ENST00000506362.1:c.749G>C
|
|
|
ENST00000507765.1:n.1301G>C
|
|
|
NM_001145853.1:c.1116G>C
|
NP_001139325.1:p.Glu372Asp
|
|
NM_006005.3:c.1116G>C
MANE Select
|
NP_005996.2:p.Glu372Asp
|
|
XM_017008586.1:c.1125G>C
|
XP_016864075.1:p.Glu375Asp
|
|