ENST00000389857.11:c.4722G>A
MANE Select
|
ENSP00000374507.6:p.Glu1574=
|
|
ENST00000331194.8:c.294G>A
|
ENSP00000330332.8:p.Glu98=
|
|
ENST00000334448.5:n.534G>A
|
|
|
ENST00000389857.10:c.4722G>A
|
ENSP00000374507.6:p.Glu1574=
|
|
ENST00000556726.5:c.950G>A
|
|
|
ENST00000557455.1:n.694G>A
|
|
|
NM_001080414.3:c.4722G>A
|
NP_001073883.2:p.Glu1574=
|
|
XM_011536796.1:c.4614G>A
|
XP_011535098.1:p.Glu1538=
|
|
XR_429316.2:n.4997G>A
|
|
|
XM_011536796.2:c.4614G>A
|
XP_011535098.1:p.Glu1538=
|
|
XM_017021336.1:c.1803G>A
|
XP_016876825.1:p.Glu601=
|
|
XR_429316.4:n.4995G>A
|
|
|
NM_001080414.4:c.4722G>A
MANE Select
|
NP_001073883.2:p.Glu1574=
|
|