ENST00000682565.1:c.11532A>T
|
ENSP00000507671.1:p.Arg3844Ser
|
|
ENST00000682801.1:c.11167-950A>T
|
ENSP00000507862.1:n.11167-950A>T
|
|
ENST00000682859.1:c.11532A>T
|
ENSP00000508222.1:p.Arg3844Ser
|
|
ENST00000683791.1:c.4618A>T
|
|
|
ENST00000684460.1:c.8813A>T
|
|
|
ENST00000684548.1:c.11532A>T
|
ENSP00000507421.1:p.Arg3844Ser
|
|
ENST00000684590.1:c.5979A>T
|
ENSP00000507376.1:p.Arg1993Ser
|
|
ENST00000684656.1:c.8997A>T
|
|
|
ENST00000613296.6:c.11913A>T
MANE Select
|
ENSP00000482968.1:p.Arg3971Ser
|
|
ENST00000651057.1:c.2067A>T
|
ENSP00000498504.1:p.Arg689Ser
|
|
ENST00000651434.1:c.3269A>T
|
|
|
ENST00000651750.1:c.1260+354A>T
|
|
|
ENST00000652487.1:c.3084A>T
|
|
|
ENST00000464408.3:n.88A>T
|
|
|
ENST00000484298.5:c.11787A>T
|
ENSP00000478155.1:p.Arg3929Ser
|
|
ENST00000613296.4:c.11913A>T
|
ENSP00000482968.1:p.Arg3971Ser
|
|
ENST00000620466.4:n.5716A>T
|
|
|
NM_015120.4:c.11916A>T , LRG_741t1:c.11916A>T
|
NP_055935.4:p.Arg3972Ser
|
|
NM_001378454.1:c.11913A>T
MANE Select
|
NP_001365383.1:p.Arg3971Ser
|
|