ENST00000493477.2:n.1553G>A
|
|
|
ENST00000682162.1:c.1079G>A
|
ENSP00000508203.1:n.1079G>A
|
|
ENST00000682567.1:n.1127G>A
|
|
|
ENST00000683521.1:c.1050G>A
|
ENSP00000506864.1:p.Arg350=
|
|
ENST00000684161.1:n.2265G>A
|
|
|
ENST00000684483.1:c.*446G>A
|
ENSP00000507894.1:n.*446G>A
|
|
ENST00000366560.4:c.1050G>A
MANE Select
|
ENSP00000355518.4:p.Arg350=
|
|
ENST00000366560.3:c.1050G>A
|
ENSP00000355518.3:p.Arg350=
|
|
NM_000143.3:c.1050G>A , LRG_504t1:c.1050G>A
|
NP_000134.2:p.Arg350=
|
|
XM_011544132.1:c.822G>A
|
XP_011542434.1:p.Arg274=
|
|
XM_011544132.2:c.822G>A
|
XP_011542434.1:p.Arg274=
|
|
NM_000143.4:c.1050G>A
MANE Select
|
NP_000134.2:p.Arg350=
|
|