ENST00000682565.1:c.11684G>C
|
ENSP00000507671.1:p.Arg3895Thr
|
|
ENST00000682801.1:c.11167-798G>C
|
ENSP00000507862.1:n.11167-798G>C
|
|
ENST00000682859.1:c.11684G>C
|
ENSP00000508222.1:p.Arg3895Thr
|
|
ENST00000683791.1:c.4770G>C
|
|
|
ENST00000684460.1:c.8965G>C
|
|
|
ENST00000684548.1:c.11684G>C
|
ENSP00000507421.1:p.Arg3895Thr
|
|
ENST00000684590.1:c.6131G>C
|
ENSP00000507376.1:p.Arg2044Thr
|
|
ENST00000684656.1:c.9149G>C
|
|
|
ENST00000613296.6:c.12065G>C
MANE Select
|
ENSP00000482968.1:p.Arg4022Thr
|
|
ENST00000651057.1:c.2219G>C
|
ENSP00000498504.1:p.Arg740Thr
|
|
ENST00000651434.1:c.3421G>C
|
|
|
ENST00000651750.1:c.1260+506G>C
|
|
|
ENST00000652487.1:c.3236G>C
|
|
|
ENST00000464408.3:n.240G>C
|
|
|
ENST00000484298.5:c.11939G>C
|
ENSP00000478155.1:p.Arg3980Thr
|
|
ENST00000613296.4:c.12065G>C
|
ENSP00000482968.1:p.Arg4022Thr
|
|
ENST00000620466.4:n.5868G>C
|
|
|
NM_015120.4:c.12068G>C , LRG_741t1:c.12068G>C
|
NP_055935.4:p.Arg4023Thr
|
|
NM_001378454.1:c.12065G>C
MANE Select
|
NP_001365383.1:p.Arg4022Thr
|
|