ENST00000703783.1:n.544G=
|
|
|
ENST00000703785.1:n.625G=
|
|
|
ENST00000262464.9:c.3760G=
MANE Select
|
ENSP00000262464.4:p.Asp1254=
|
|
ENST00000262464.8:c.3760G=
|
ENSP00000262464.4:p.Asp1254=
|
|
ENST00000507835.5:c.310G=
|
ENSP00000426839.1:p.Asp104=
|
|
ENST00000508053.5:c.3760G=
|
ENSP00000424571.1:p.Asp1254=
|
|
ENST00000508989.5:c.3661G=
|
ENSP00000425596.1:p.Asp1221=
|
|
ENST00000619499.4:c.3757G=
|
ENSP00000482132.1:p.Asp1253=
|
|
NM_001999.3:c.3760G=
|
NP_001990.2:p.Asp1254=
|
|
XM_017009228.2:c.3607G=
|
XP_016864717.1:p.Asp1203=
|
|
NM_001999.4:c.3760G=
MANE Select
|
NP_001990.2:p.Asp1254=
|
|