ENST00000682565.1:c.10593A>C
|
ENSP00000507671.1:p.Arg3531=
|
|
ENST00000682801.1:c.10593A>C
|
ENSP00000507862.1:p.Arg3531=
|
|
ENST00000682859.1:c.10593A>C
|
ENSP00000508222.1:p.Arg3531=
|
|
ENST00000683791.1:c.3679A>C
|
|
|
ENST00000684460.1:c.7874A>C
|
|
|
ENST00000684548.1:c.10593A>C
|
ENSP00000507421.1:p.Arg3531=
|
|
ENST00000684590.1:c.5040A>C
|
ENSP00000507376.1:p.Arg1680=
|
|
ENST00000684656.1:c.7919A>C
|
|
|
ENST00000613296.6:c.10974A>C
MANE Select
|
ENSP00000482968.1:p.Arg3658=
|
|
ENST00000651057.1:c.1128A>C
|
ENSP00000498504.1:p.Arg376=
|
|
ENST00000651434.1:c.2330A>C
|
|
|
ENST00000651750.1:c.362A>C
|
|
|
ENST00000652487.1:c.2071A>C
|
|
|
ENST00000423048.5:c.4465A>C
|
ENSP00000399833.1:n.4465A>C
|
|
ENST00000484298.5:c.10848A>C
|
ENSP00000478155.1:p.Arg3616=
|
|
ENST00000613296.4:c.10974A>C
|
ENSP00000482968.1:p.Arg3658=
|
|
ENST00000614410.4:c.10974A>C
|
ENSP00000479094.1:p.Arg3658=
|
|
ENST00000620466.4:n.4777A>C
|
|
|
NM_015120.4:c.10977A>C , LRG_741t1:c.10977A>C
|
NP_055935.4:p.Arg3659=
|
|
NM_001378454.1:c.10974A>C
MANE Select
|
NP_001365383.1:p.Arg3658=
|
|