ENST00000313468.10:c.324G>T
MANE Select
|
ENSP00000315774.5:p.Glu108Asp
|
|
ENST00000313468.9:c.324G>T
|
ENSP00000315774.5:p.Glu108Asp
|
|
ENST00000432321.6:n.441G>T
|
|
|
ENST00000453471.6:c.324G>T
|
ENSP00000403972.2:p.Glu108Asp
|
|
ENST00000524810.5:c.95G>T
|
|
|
ENST00000525419.5:c.270G>T
|
ENSP00000433521.1:p.Glu90Asp
|
|
ENST00000525628.1:c.324G>T
|
ENSP00000432968.1:p.Glu108Asp
|
|
ENST00000526339.5:c.324G>T
|
ENSP00000436287.1:p.Glu108Asp
|
|
ENST00000526446.5:c.*379G>T
|
ENSP00000433645.1:n.*379G>T
|
|
ENST00000528492.1:c.-67+2502G>T
|
ENSP00000432848.1:n.-67+2502G>T
|
|
ENST00000529645.1:c.502G>T
|
ENSP00000431293.1:n.502G>T
|
|
ENST00000532399.1:n.1029G>T
|
|
|
NM_002496.3:c.324G>T
|
NP_002487.1:p.Glu108Asp
|
|
XM_005274013.1:c.324G>T
|
XP_005274070.1:p.Glu108Asp
|
|
XM_005274014.1:c.324G>T
|
XP_005274071.1:p.Glu108Asp
|
|
XM_005274015.1:c.204G>T
|
XP_005274072.1:p.Glu68Asp
|
|
XM_011545053.1:c.324G>T
|
XP_011543355.1:p.Glu108Asp
|
|
NM_002496.4:c.324G>T
MANE Select
|
NP_002487.1:p.Glu108Asp
|
|