ENST00000348974.5:c.867T=
|
ENSP00000330021.7:p.Leu289=
|
|
ENST00000394236.9:c.867T=
MANE Select
|
ENSP00000377783.3:p.Leu289=
|
|
ENST00000407433.6:c.822T=
|
ENSP00000385794.2:p.Leu274=
|
|
ENST00000647936.1:c.867T=
|
ENSP00000496822.1:p.Leu289=
|
|
ENST00000648381.1:n.1035T=
|
|
|
ENST00000648853.1:c.825T=
|
ENSP00000497262.1:p.Leu275=
|
|
ENST00000649103.1:c.966T=
|
ENSP00000497962.1:n.966T=
|
|
ENST00000650591.1:c.963T=
|
ENSP00000497376.1:p.Leu321=
|
|
ENST00000394236.7:c.867T=
|
ENSP00000377783.3:p.Leu289=
|
|
ENST00000407433.5:c.474T=
|
ENSP00000385794.1:p.Leu158=
|
|
NM_000313.3:c.867T= , LRG_572t1:c.867T=
|
NP_000304.2:p.Leu289=
|
|
NM_001314077.1:c.963T= , LRG_572t2:c.963T=
|
NP_001301006.1:p.Leu321=
|
|
NM_000313.4:c.867T=
MANE Select
|
NP_000304.2:p.Leu289=
|
|
NM_001314077.2:c.963T=
|
NP_001301006.1:p.Leu321=
|
|