ENST00000493477.2:n.1479G=
|
|
|
ENST00000682162.1:c.1005G=
|
ENSP00000508203.1:n.1005G=
|
|
ENST00000682567.1:n.1053G=
|
|
|
ENST00000683521.1:c.976G=
|
ENSP00000506864.1:p.Gly326=
|
|
ENST00000684161.1:n.2191G=
|
|
|
ENST00000684483.1:c.*372G=
|
ENSP00000507894.1:n.*372G=
|
|
ENST00000366560.4:c.976G=
MANE Select
|
ENSP00000355518.4:p.Gly326=
|
|
ENST00000366560.3:c.976G=
|
ENSP00000355518.3:p.Gly326=
|
|
NM_000143.3:c.976G= , LRG_504t1:c.976G=
|
NP_000134.2:p.Gly326=
|
|
XM_011544132.1:c.748G=
|
XP_011542434.1:p.Gly250=
|
|
XM_011544132.2:c.748G=
|
XP_011542434.1:p.Gly250=
|
|
NM_000143.4:c.976G=
MANE Select
|
NP_000134.2:p.Gly326=
|
|