ENST00000389857.11:c.4704G>C
MANE Select
|
ENSP00000374507.6:p.Ser1568=
|
|
ENST00000331194.8:c.276G>C
|
ENSP00000330332.8:p.Ser92=
|
|
ENST00000334448.5:n.516G>C
|
|
|
ENST00000389857.10:c.4704G>C
|
ENSP00000374507.6:p.Ser1568=
|
|
ENST00000556726.5:c.932G>C
|
|
|
ENST00000557455.1:n.676G>C
|
|
|
NM_001080414.3:c.4704G>C
|
NP_001073883.2:p.Ser1568=
|
|
XM_011536796.1:c.4596G>C
|
XP_011535098.1:p.Ser1532=
|
|
XR_429316.2:n.4979G>C
|
|
|
XM_011536796.2:c.4596G>C
|
XP_011535098.1:p.Ser1532=
|
|
XM_017021336.1:c.1785G>C
|
XP_016876825.1:p.Ser595=
|
|
XR_429316.4:n.4977G>C
|
|
|
NM_001080414.4:c.4704G>C
MANE Select
|
NP_001073883.2:p.Ser1568=
|
|