ENST00000493477.2:n.992A>T
|
|
|
ENST00000682162.1:c.518A>T
|
ENSP00000508203.1:n.518A>T
|
|
ENST00000682567.1:n.566A>T
|
|
|
ENST00000683521.1:c.489A>T
|
ENSP00000506864.1:p.Glu163Asp
|
|
ENST00000684483.1:c.489A>T
|
ENSP00000507894.1:p.Glu163Asp
|
|
ENST00000366560.4:c.489A>T
MANE Select
|
ENSP00000355518.4:p.Glu163Asp
|
|
ENST00000366560.3:c.489A>T
|
ENSP00000355518.3:p.Glu163Asp
|
|
ENST00000497042.1:n.185A>T
|
|
|
NM_000143.3:c.489A>T , LRG_504t1:c.489A>T
|
NP_000134.2:p.Glu163Asp
|
|
XM_011544132.1:c.261A>T
|
XP_011542434.1:p.Glu87Asp
|
|
XM_011544132.2:c.261A>T
|
XP_011542434.1:p.Glu87Asp
|
|
NM_000143.4:c.489A>T
MANE Select
|
NP_000134.2:p.Glu163Asp
|
|