ENST00000493477.2:n.990G>T
|
|
|
ENST00000682162.1:c.516G>T
|
ENSP00000508203.1:n.516G>T
|
|
ENST00000682567.1:n.564G>T
|
|
|
ENST00000683521.1:c.487G>T
|
ENSP00000506864.1:p.Glu163Ter
|
|
ENST00000684483.1:c.487G>T
|
ENSP00000507894.1:p.Glu163Ter
|
|
ENST00000366560.4:c.487G>T
MANE Select
|
ENSP00000355518.4:p.Glu163Ter
|
|
ENST00000366560.3:c.487G>T
|
ENSP00000355518.3:p.Glu163Ter
|
|
ENST00000497042.1:n.183G>T
|
|
|
NM_000143.3:c.487G>T , LRG_504t1:c.487G>T
|
NP_000134.2:p.Glu163Ter
|
|
XM_011544132.1:c.259G>T
|
XP_011542434.1:p.Glu87Ter
|
|
XM_011544132.2:c.259G>T
|
XP_011542434.1:p.Glu87Ter
|
|
NM_000143.4:c.487G>T
MANE Select
|
NP_000134.2:p.Glu163Ter
|
|