ENST00000696142.1:c.*274G>T
|
ENSP00000512434.1:n.*274G>T
|
|
ENST00000696143.1:c.733G>T
|
ENSP00000512435.1:n.733G>T
|
|
ENST00000696153.1:c.708G>T
|
ENSP00000512444.1:p.Glu236Asp
|
|
ENST00000256474.3:c.597G>T
MANE Select
|
ENSP00000256474.3:p.Glu199Asp
|
|
ENST00000256474.2:c.597G>T
|
ENSP00000256474.2:p.Glu199Asp
|
|
ENST00000345392.2:c.474G>T
|
ENSP00000344757.2:p.Glu158Asp
|
|
ENST00000477538.1:n.733G>T
|
|
|
NM_000551.3:c.597G>T , LRG_322t1:c.597G>T
|
NP_000542.1:p.Glu199Asp
|
|
NM_198156.2:c.474G>T
|
NP_937799.1:p.Glu158Asp
|
|
NM_001354723.1:c.*151G>T
|
NP_001341652.1:n.*151G>T
|
|
NM_000551.4:c.597G>T
MANE Select
|
NP_000542.1:p.Glu199Asp
|
|
NM_001354723.2:c.*151G>T
|
NP_001341652.1:n.*151G>T
|
|
NM_198156.3:c.474G>T
|
NP_937799.1:p.Glu158Asp
|
|