ENST00000389857.11:c.5112C=
MANE Select
|
ENSP00000374507.6:p.Ser1704=
|
|
ENST00000331194.8:c.684C=
|
ENSP00000330332.8:p.Ser228=
|
|
ENST00000334448.5:n.924C=
|
|
|
ENST00000389857.10:c.5112C=
|
ENSP00000374507.6:p.Ser1704=
|
|
ENST00000556726.5:c.1340C=
|
|
|
NM_001080414.3:c.5112C=
|
NP_001073883.2:p.Ser1704=
|
|
XM_011536796.1:c.5004C=
|
XP_011535098.1:p.Ser1668=
|
|
XR_429316.2:n.5387C=
|
|
|
XM_011536796.2:c.5004C=
|
XP_011535098.1:p.Ser1668=
|
|
XM_017021336.1:c.2193C=
|
XP_016876825.1:p.Ser731=
|
|
XR_429316.4:n.5385C=
|
|
|
NM_001080414.4:c.5112C=
MANE Select
|
NP_001073883.2:p.Ser1704=
|
|