ENST00000493477.2:n.1208T=
|
|
|
ENST00000682162.1:c.734T=
|
ENSP00000508203.1:n.734T=
|
|
ENST00000682567.1:n.782T=
|
|
|
ENST00000683521.1:c.705T=
|
ENSP00000506864.1:p.His235=
|
|
ENST00000684161.1:n.1920T=
|
|
|
ENST00000684483.1:c.*101T=
|
ENSP00000507894.1:n.*101T=
|
|
ENST00000366560.4:c.705T=
MANE Select
|
ENSP00000355518.4:p.His235=
|
|
ENST00000366560.3:c.705T=
|
ENSP00000355518.3:p.His235=
|
|
NM_000143.3:c.705T= , LRG_504t1:c.705T=
|
NP_000134.2:p.His235=
|
|
XM_011544132.1:c.477T=
|
XP_011542434.1:p.His159=
|
|
XM_011544132.2:c.477T=
|
XP_011542434.1:p.His159=
|
|
NM_000143.4:c.705T=
MANE Select
|
NP_000134.2:p.His235=
|
|