ENST00000480266.6:c.681C>T
|
ENSP00000479015.1:p.Tyr227=
|
|
ENST00000373203.9:c.1227C>T
MANE Select
|
ENSP00000362299.4:p.Tyr409=
|
|
ENST00000344849.4:c.1227C>T
|
ENSP00000341917.3:p.Tyr409=
|
|
ENST00000373203.8:c.1227C>T
|
ENSP00000362299.4:p.Tyr409=
|
|
ENST00000480266.5:c.681C>T
|
ENSP00000479015.1:p.Tyr227=
|
|
ENST00000486329.1:n.195C>T
|
|
|
NM_000118.3:c.1227C>T , LRG_589t1:c.1227C>T
|
NP_000109.1:p.Tyr409=
|
|
NM_001114753.2:c.1227C>T , LRG_589t2:c.1227C>T
|
NP_001108225.1:p.Tyr409=
|
|
NM_001278138.1:c.681C>T
|
NP_001265067.1:p.Tyr227=
|
|
NR_136302.1:n.1568+1234G>A
|
|
|
NM_001114753.3:c.1227C>T
MANE Select
|
NP_001108225.1:p.Tyr409=
|
|
NM_001278138.2:c.681C>T
|
NP_001265067.1:p.Tyr227=
|
|