ENST00000295897.9:c.1483_1485delinsGAC
MANE Select
|
ENSP00000295897.4:p.Asp495=
|
|
ENST00000295897.8:c.1483_1485delinsGAC
|
ENSP00000295897.4:p.Asp495=
|
|
ENST00000401494.7:c.1138_1140delinsGAC
|
ENSP00000384695.3:p.Asp380=
|
|
ENST00000415165.6:c.907_909delinsGAC
|
ENSP00000401820.2:p.Asp303=
|
|
ENST00000476441.6:c.*762_*764delinsGAC
|
ENSP00000423727.1:n.*762_*764delinsGAC
|
|
ENST00000486939.1:n.137_139delinsGAC
|
|
|
ENST00000503124.5:c.1033_1035delinsGAC
|
ENSP00000421027.1:p.Asp345=
|
|
ENST00000505649.5:n.1030_1032delinsGAC
|
|
|
ENST00000509063.5:c.1483_1485delinsGAC
|
ENSP00000422784.1:p.Asp495=
|
|
ENST00000511370.1:c.1016_1018delinsGAC
|
|
|
ENST00000621085.4:c.844_846delinsGAC
|
ENSP00000483421.1:p.Asp282=
|
|
ENST00000621628.4:c.844_846delinsGAC
|
ENSP00000480485.1:p.Asp282=
|
|
NM_000477.5:c.1483_1485delinsGAC
|
NP_000468.1:p.Asp495=
|
|
NM_000477.6:c.1483_1485delinsGAC
|
NP_000468.1:p.Asp495=
|
|
NM_000477.7:c.1483_1485delinsGAC
MANE Select
|
NP_000468.1:p.Asp495=
|
|