ENST00000696142.1:c.*157G>T
|
ENSP00000512434.1:n.*157G>T
|
|
ENST00000696143.1:c.616G>T
|
ENSP00000512435.1:n.616G>T
|
|
ENST00000696153.1:c.591G>T
|
ENSP00000512444.1:p.Glu197Asp
|
|
ENST00000256474.3:c.480G>T
MANE Select
|
ENSP00000256474.3:p.Glu160Asp
|
|
ENST00000256474.2:c.480G>T
|
ENSP00000256474.2:p.Glu160Asp
|
|
ENST00000345392.2:c.357G>T
|
ENSP00000344757.2:p.Glu119Asp
|
|
ENST00000477538.1:n.616G>T
|
|
|
NM_000551.3:c.480G>T , LRG_322t1:c.480G>T
|
NP_000542.1:p.Glu160Asp
|
|
NM_198156.2:c.357G>T
|
NP_937799.1:p.Glu119Asp
|
|
NM_001354723.1:c.*34G>T
|
NP_001341652.1:n.*34G>T
|
|
NM_000551.4:c.480G>T
MANE Select
|
NP_000542.1:p.Glu160Asp
|
|
NM_001354723.2:c.*34G>T
|
NP_001341652.1:n.*34G>T
|
|
NM_198156.3:c.357G>T
|
NP_937799.1:p.Glu119Asp
|
|