ENST00000205402.10:c.740A=
MANE Select
|
ENSP00000205402.3:p.His247=
|
|
ENST00000205402.9:c.740A=
|
ENSP00000205402.3:p.His247=
|
|
ENST00000415325.5:c.*414A=
|
ENSP00000402593.1:n.*414A=
|
|
ENST00000417551.5:c.740A=
|
ENSP00000390667.1:p.His247=
|
|
ENST00000437604.6:c.596A=
|
ENSP00000387542.2:p.His199=
|
|
ENST00000440410.5:c.671A=
|
ENSP00000417016.1:p.His224=
|
|
ENST00000451081.5:c.*483A=
|
ENSP00000388077.1:n.*483A=
|
|
NM_000108.4:c.740A=
|
NP_000099.2:p.His247=
|
|
NM_001289750.1:c.443A=
|
NP_001276679.1:p.His148=
|
|
NM_001289751.1:c.671A=
|
NP_001276680.1:p.His224=
|
|
NM_001289752.1:c.596A=
|
NP_001276681.1:p.His199=
|
|
NM_000108.5:c.740A=
MANE Select
|
NP_000099.2:p.His247=
|
|