ENST00000273283.7:c.1744G=
MANE Select
|
ENSP00000273283.2:p.Asp582=
|
|
ENST00000273283.6:c.1744G=
|
ENSP00000273283.2:p.Asp582=
|
|
ENST00000428133.5:c.403G=
|
ENSP00000395836.1:p.Asp135=
|
|
ENST00000484844.2:c.11G=
|
|
|
ENST00000537050.5:c.880G=
|
ENSP00000443847.1:p.Asp294=
|
|
ENST00000628722.2:n.1599G=
|
|
|
NM_001166434.2:c.1318G=
|
NP_001159906.1:p.Asp440=
|
|
NM_001166435.2:c.880G=
|
NP_001159907.1:p.Asp294=
|
|
NM_001166436.2:c.880G=
|
NP_001159908.1:p.Asp294=
|
|
NM_002215.3:c.1744G=
|
NP_002206.2:p.Asp582=
|
|
NM_002215.4:c.1744G=
MANE Select
|
NP_002206.2:p.Asp582=
|
|
NM_001166434.3:c.1318G=
|
NP_001159906.1:p.Asp440=
|
|