ENST00000674537.2:c.1180G>T
|
ENSP00000502725.1:p.Ala394Ser
|
|
ENST00000392302.7:c.1180G>T
|
ENSP00000376120.3:p.Ala394Ser
|
|
ENST00000497019.7:c.1047G>T
|
ENSP00000436804.2:p.Arg349=
|
|
ENST00000524377.7:c.1360G>T
MANE Select
|
ENSP00000431418.1:p.Ala454Ser
|
|
ENST00000674537.1:c.1180G>T
|
ENSP00000502725.1:p.Ala394Ser
|
|
ENST00000358660.3:c.1342G>T
|
ENSP00000351486.3:p.Ala448Ser
|
|
ENST00000368196.7:c.1342G>T
|
ENSP00000357179.3:p.Ala448Ser
|
|
ENST00000392302.6:c.1252G>T
|
ENSP00000376120.2:p.Ala418Ser
|
|
ENST00000497019.6:c.1119G>T
|
ENSP00000436804.1:p.Arg373=
|
|
ENST00000524377.5:c.1360G>T
|
ENSP00000431418.1:p.Ala454Ser
|
|
ENST00000530298.5:n.1400G>T
|
|
|
ENST00000534682.1:n.583G>T
|
|
|
NM_001007792.1:c.1252G>T , LRG_261t1:c.1252G>T
|
NP_001007793.1:p.Ala418Ser
|
|
NM_001012331.1:c.1342G>T , LRG_261t2:c.1342G>T
|
NP_001012331.1:p.Ala448Ser
|
|
NM_002529.3:c.1360G>T , LRG_261t3:c.1360G>T
|
NP_002520.2:p.Ala454Ser
|
|
NM_001012331.2:c.1342G>T
|
NP_001012331.1:p.Ala448Ser
|
|
NM_002529.4:c.1360G>T
MANE Select
|
NP_002520.2:p.Ala454Ser
|
|