ENST00000348974.5:c.1679A=
|
ENSP00000330021.7:p.Tyr560=
|
|
ENST00000394236.9:c.1679A=
MANE Select
|
ENSP00000377783.3:p.Tyr560=
|
|
ENST00000407433.6:c.1634A=
|
ENSP00000385794.2:p.Tyr545=
|
|
ENST00000647936.1:c.1644+2006A=
|
ENSP00000496822.1:n.1644+2006A=
|
|
ENST00000648381.1:n.1847A=
|
|
|
ENST00000648853.1:c.1637A=
|
ENSP00000497262.1:p.Tyr546=
|
|
ENST00000649103.1:c.1778A=
|
ENSP00000497962.1:n.1778A=
|
|
ENST00000649585.1:c.622A=
|
ENSP00000498163.1:n.622A=
|
|
ENST00000650591.1:c.1775A=
|
ENSP00000497376.1:p.Tyr592=
|
|
ENST00000394236.7:c.1679A=
|
ENSP00000377783.3:p.Tyr560=
|
|
ENST00000407433.5:c.1286A=
|
ENSP00000385794.1:p.Tyr429=
|
|
NM_000313.3:c.1679A= , LRG_572t1:c.1679A=
|
NP_000304.2:p.Tyr560=
|
|
NM_001314077.1:c.1775A= , LRG_572t2:c.1775A=
|
NP_001301006.1:p.Tyr592=
|
|
NM_000313.4:c.1679A=
MANE Select
|
NP_000304.2:p.Tyr560=
|
|
NM_001314077.2:c.1775A=
|
NP_001301006.1:p.Tyr592=
|
|