ENST00000474370.2:n.2389A=
|
|
|
ENST00000492391.2:n.1540A=
|
|
|
ENST00000682645.1:n.3487A=
|
|
|
ENST00000683432.1:c.*591A=
|
ENSP00000508174.1:n.*591A=
|
|
ENST00000684207.1:c.416A=
|
ENSP00000506942.1:p.Asp139=
|
|
ENST00000297157.8:c.416A=
MANE Select
|
ENSP00000297157.3:p.Asp139=
|
|
ENST00000297157.7:c.416A=
|
ENSP00000297157.3:p.Asp139=
|
|
ENST00000448915.1:c.314A=
|
ENSP00000411577.1:p.Asp105=
|
|
NM_203288.1:c.416A=
|
NP_976033.1:p.Asp139=
|
|
XM_011515468.1:c.314A=
|
XP_011513770.1:p.Asp105=
|
|
XM_011515468.3:c.314A=
|
XP_011513770.1:p.Asp105=
|
|
NM_203288.2:c.416A=
MANE Select
|
NP_976033.1:p.Asp139=
|
|