ENST00000442561.7:c.255C>A
MANE Select
|
ENSP00000406970.2:p.Thr85=
|
|
ENST00000367215.1:n.225C>A
|
|
|
ENST00000367217.5:c.207C>A
|
ENSP00000356186.5:p.Thr69=
|
|
ENST00000442561.6:c.255C>A
|
ENSP00000406970.2:p.Thr85=
|
|
NM_001136190.1:c.207C>A
|
NP_001129662.1:p.Thr69=
|
|
NM_001282878.1:c.27C>A
|
NP_001269807.1:p.Thr9=
|
|
NM_017773.3:c.255C>A
|
NP_060243.2:p.Thr85=
|
|
XM_006711397.2:c.255C>A
|
XP_006711460.1:p.Thr85=
|
|
XM_006711397.3:c.255C>A
|
XP_006711460.1:p.Thr85=
|
|
NM_001136190.2:c.207C>A
|
NP_001129662.1:p.Thr69=
|
|
NM_017773.4:c.255C>A
MANE Select
|
NP_060243.2:p.Thr85=
|
|