ENST00000493477.2:n.1138A>G
|
|
|
ENST00000682162.1:c.664A>G
|
ENSP00000508203.1:n.664A>G
|
|
ENST00000682567.1:n.712A>G
|
|
|
ENST00000683521.1:c.635A>G
|
ENSP00000506864.1:p.Gln212Arg
|
|
ENST00000684161.1:n.1850A>G
|
|
|
ENST00000684483.1:c.*31A>G
|
ENSP00000507894.1:n.*31A>G
|
|
ENST00000366560.4:c.635A>G
MANE Select
|
ENSP00000355518.4:p.Gln212Arg
|
|
ENST00000366560.3:c.635A>G
|
ENSP00000355518.3:p.Gln212Arg
|
|
NM_000143.3:c.635A>G , LRG_504t1:c.635A>G
|
NP_000134.2:p.Gln212Arg
|
|
XM_011544132.1:c.407A>G
|
XP_011542434.1:p.Gln136Arg
|
|
XM_011544132.2:c.407A>G
|
XP_011542434.1:p.Gln136Arg
|
|
NM_000143.4:c.635A>G
MANE Select
|
NP_000134.2:p.Gln212Arg
|
|