ENST00000703783.1:n.350A=
|
|
|
ENST00000703785.1:n.431A=
|
|
|
ENST00000262464.9:c.3566A=
MANE Select
|
ENSP00000262464.4:p.His1189=
|
|
ENST00000262464.8:c.3566A=
|
ENSP00000262464.4:p.His1189=
|
|
ENST00000507835.5:c.116A=
|
ENSP00000426839.1:p.His39=
|
|
ENST00000508053.5:c.3566A=
|
ENSP00000424571.1:p.His1189=
|
|
ENST00000508989.5:c.3467A=
|
ENSP00000425596.1:p.His1156=
|
|
ENST00000619499.4:c.3563A=
|
ENSP00000482132.1:p.His1188=
|
|
NM_001999.3:c.3566A=
|
NP_001990.2:p.His1189=
|
|
XM_017009228.2:c.3413A=
|
XP_016864717.1:p.His1138=
|
|
NM_001999.4:c.3566A=
MANE Select
|
NP_001990.2:p.His1189=
|
|