ENST00000682565.1:c.7599T=
|
ENSP00000507671.1:p.Asp2533=
|
|
ENST00000682801.1:c.7599T=
|
ENSP00000507862.1:p.Asp2533=
|
|
ENST00000682859.1:c.7599T=
|
ENSP00000508222.1:p.Asp2533=
|
|
ENST00000683791.1:c.991T=
|
|
|
ENST00000684460.1:c.5051T=
|
|
|
ENST00000684548.1:c.7599T=
|
ENSP00000507421.1:p.Asp2533=
|
|
ENST00000684590.1:c.2046T=
|
ENSP00000507376.1:p.Asp682=
|
|
ENST00000684656.1:c.5051T=
|
|
|
ENST00000613296.6:c.7980T=
MANE Select
|
ENSP00000482968.1:p.Asp2660=
|
|
ENST00000651434.1:c.896-29836T=
|
|
|
ENST00000423048.5:c.2811T=
|
ENSP00000399833.1:p.Asp937=
|
|
ENST00000484298.5:c.7854T=
|
ENSP00000478155.1:p.Asp2618=
|
|
ENST00000613296.4:c.7980T=
|
ENSP00000482968.1:p.Asp2660=
|
|
ENST00000614410.4:c.7980T=
|
ENSP00000479094.1:p.Asp2660=
|
|
ENST00000620466.4:n.1783T=
|
|
|
NM_015120.4:c.7983T= , LRG_741t1:c.7983T=
|
NP_055935.4:p.Asp2661=
|
|
NM_001378454.1:c.7980T=
MANE Select
|
NP_001365383.1:p.Asp2660=
|
|