ENST00000389857.11:c.5079T>C
MANE Select
|
ENSP00000374507.6:p.Asp1693=
|
|
ENST00000331194.8:c.651T>C
|
ENSP00000330332.8:p.Asp217=
|
|
ENST00000334448.5:n.891T>C
|
|
|
ENST00000389857.10:c.5079T>C
|
ENSP00000374507.6:p.Asp1693=
|
|
ENST00000556726.5:c.1307T>C
|
|
|
NM_001080414.3:c.5079T>C
|
NP_001073883.2:p.Asp1693=
|
|
XM_011536796.1:c.4971T>C
|
XP_011535098.1:p.Asp1657=
|
|
XR_429316.2:n.5354T>C
|
|
|
XM_011536796.2:c.4971T>C
|
XP_011535098.1:p.Asp1657=
|
|
XM_017021336.1:c.2160T>C
|
XP_016876825.1:p.Asp720=
|
|
XR_429316.4:n.5352T>C
|
|
|
NM_001080414.4:c.5079T>C
MANE Select
|
NP_001073883.2:p.Asp1693=
|
|