ENST00000674537.2:c.1686G>C
|
ENSP00000502725.1:p.Leu562=
|
|
ENST00000392302.7:c.1686G>C
|
ENSP00000376120.3:p.Leu562=
|
|
ENST00000497019.7:c.*458G>C
|
ENSP00000436804.2:n.*458G>C
|
|
ENST00000524377.7:c.1866G>C
MANE Select
|
ENSP00000431418.1:p.Leu622=
|
|
ENST00000674537.1:c.1686G>C
|
ENSP00000502725.1:p.Leu562=
|
|
ENST00000358660.3:c.1857G>C
|
ENSP00000351486.3:p.Leu619=
|
|
ENST00000368196.7:c.1848G>C
|
ENSP00000357179.3:p.Leu616=
|
|
ENST00000392302.6:c.1758G>C
|
ENSP00000376120.2:p.Leu586=
|
|
ENST00000497019.6:c.*458G>C
|
ENSP00000436804.1:n.*458G>C
|
|
ENST00000524377.5:c.1866G>C
|
ENSP00000431418.1:p.Leu622=
|
|
ENST00000530298.5:n.2319G>C
|
|
|
NM_001007792.1:c.1758G>C , LRG_261t1:c.1758G>C
|
NP_001007793.1:p.Leu586=
|
|
NM_001012331.1:c.1848G>C , LRG_261t2:c.1848G>C
|
NP_001012331.1:p.Leu616=
|
|
NM_002529.3:c.1866G>C , LRG_261t3:c.1866G>C
|
NP_002520.2:p.Leu622=
|
|
NM_001012331.2:c.1848G>C
|
NP_001012331.1:p.Leu616=
|
|
NM_002529.4:c.1866G>C
MANE Select
|
NP_002520.2:p.Leu622=
|
|