ENST00000682565.1:c.10249A>C
|
ENSP00000507671.1:p.Arg3417=
|
|
ENST00000682801.1:c.10249A>C
|
ENSP00000507862.1:p.Arg3417=
|
|
ENST00000682859.1:c.10249A>C
|
ENSP00000508222.1:p.Arg3417=
|
|
ENST00000683791.1:c.3335A>C
|
|
|
ENST00000684460.1:c.7530A>C
|
|
|
ENST00000684548.1:c.10249A>C
|
ENSP00000507421.1:p.Arg3417=
|
|
ENST00000684590.1:c.4696A>C
|
ENSP00000507376.1:p.Arg1566=
|
|
ENST00000684656.1:c.7575A>C
|
|
|
ENST00000613296.6:c.10630A>C
MANE Select
|
ENSP00000482968.1:p.Arg3544=
|
|
ENST00000651057.1:c.784A>C
|
ENSP00000498504.1:p.Arg262=
|
|
ENST00000651434.1:c.1986A>C
|
|
|
ENST00000651750.1:c.18A>C
|
|
|
ENST00000652487.1:c.1727A>C
|
|
|
ENST00000423048.5:c.4121A>C
|
ENSP00000399833.1:n.4121A>C
|
|
ENST00000484298.5:c.10504A>C
|
ENSP00000478155.1:p.Arg3502=
|
|
ENST00000613296.4:c.10630A>C
|
ENSP00000482968.1:p.Arg3544=
|
|
ENST00000614410.4:c.10630A>C
|
ENSP00000479094.1:p.Arg3544=
|
|
ENST00000620466.4:n.4433A>C
|
|
|
NM_015120.4:c.10633A>C , LRG_741t1:c.10633A>C
|
NP_055935.4:p.Arg3545=
|
|
NM_001378454.1:c.10630A>C
MANE Select
|
NP_001365383.1:p.Arg3544=
|
|