ENST00000682565.1:c.11685A>T
|
ENSP00000507671.1:p.Arg3895Ser
|
|
ENST00000682801.1:c.11167-797A>T
|
ENSP00000507862.1:n.11167-797A>T
|
|
ENST00000682859.1:c.11685A>T
|
ENSP00000508222.1:p.Arg3895Ser
|
|
ENST00000683791.1:c.4771A>T
|
|
|
ENST00000684460.1:c.8966A>T
|
|
|
ENST00000684548.1:c.11685A>T
|
ENSP00000507421.1:p.Arg3895Ser
|
|
ENST00000684590.1:c.6132A>T
|
ENSP00000507376.1:p.Arg2044Ser
|
|
ENST00000684656.1:c.9150A>T
|
|
|
ENST00000613296.6:c.12066A>T
MANE Select
|
ENSP00000482968.1:p.Arg4022Ser
|
|
ENST00000651057.1:c.2220A>T
|
ENSP00000498504.1:p.Arg740Ser
|
|
ENST00000651434.1:c.3422A>T
|
|
|
ENST00000651750.1:c.1260+507A>T
|
|
|
ENST00000652487.1:c.3237A>T
|
|
|
ENST00000464408.3:n.241A>T
|
|
|
ENST00000484298.5:c.11940A>T
|
ENSP00000478155.1:p.Arg3980Ser
|
|
ENST00000613296.4:c.12066A>T
|
ENSP00000482968.1:p.Arg4022Ser
|
|
ENST00000620466.4:n.5869A>T
|
|
|
NM_015120.4:c.12069A>T , LRG_741t1:c.12069A>T
|
NP_055935.4:p.Arg4023Ser
|
|
NM_001378454.1:c.12066A>T
MANE Select
|
NP_001365383.1:p.Arg4022Ser
|
|