ENST00000493477.2:n.1477G=
|
|
|
ENST00000682162.1:c.1003G=
|
ENSP00000508203.1:n.1003G=
|
|
ENST00000682567.1:n.1051G=
|
|
|
ENST00000683521.1:c.974G=
|
ENSP00000506864.1:p.Ser325=
|
|
ENST00000684161.1:n.2189G=
|
|
|
ENST00000684483.1:c.*370G=
|
ENSP00000507894.1:n.*370G=
|
|
ENST00000366560.4:c.974G=
MANE Select
|
ENSP00000355518.4:p.Ser325=
|
|
ENST00000366560.3:c.974G=
|
ENSP00000355518.3:p.Ser325=
|
|
NM_000143.3:c.974G= , LRG_504t1:c.974G=
|
NP_000134.2:p.Ser325=
|
|
XM_011544132.1:c.746G=
|
XP_011542434.1:p.Ser249=
|
|
XM_011544132.2:c.746G=
|
XP_011542434.1:p.Ser249=
|
|
NM_000143.4:c.974G=
MANE Select
|
NP_000134.2:p.Ser325=
|
|