ENST00000696142.1:c.*157G=
|
ENSP00000512434.1:n.*157G=
|
|
ENST00000696143.1:c.616G=
|
ENSP00000512435.1:n.616G=
|
|
ENST00000696153.1:c.591G=
|
ENSP00000512444.1:p.Glu197=
|
|
ENST00000256474.3:c.480G=
MANE Select
|
ENSP00000256474.3:p.Glu160=
|
|
ENST00000256474.2:c.480G=
|
ENSP00000256474.2:p.Glu160=
|
|
ENST00000345392.2:c.357G=
|
ENSP00000344757.2:p.Glu119=
|
|
ENST00000477538.1:n.616G=
|
|
|
NM_000551.3:c.480G= , LRG_322t1:c.480G=
|
NP_000542.1:p.Glu160=
|
|
NM_198156.2:c.357G=
|
NP_937799.1:p.Glu119=
|
|
NM_001354723.1:c.*34G=
|
NP_001341652.1:n.*34G=
|
|
NM_000551.4:c.480G=
MANE Select
|
NP_000542.1:p.Glu160=
|
|
NM_001354723.2:c.*34G=
|
NP_001341652.1:n.*34G=
|
|
NM_198156.3:c.357G=
|
NP_937799.1:p.Glu119=
|
|