ENST00000388958.8:c.618G>A
|
ENSP00000373610.3:p.Glu206=
|
|
ENST00000646100.2:c.618G>A
MANE Select
|
ENSP00000496564.2:p.Glu206=
|
|
ENST00000647277.1:c.618G>A
|
ENSP00000495594.1:p.Glu206=
|
|
ENST00000286149.8:c.618G>A
|
ENSP00000286149.4:p.Glu206=
|
|
ENST00000388956.8:c.381G>A
|
ENSP00000373608.4:p.Glu127=
|
|
ENST00000388958.7:c.618G>A
|
ENSP00000373610.3:p.Glu206=
|
|
NM_001161683.1:c.381G>A
|
NP_001155155.1:p.Glu127=
|
|
NM_144672.3:c.618G>A
|
NP_653273.3:p.Glu206=
|
|
XM_011545747.1:c.618G>A
|
XP_011544049.1:p.Glu206=
|
|
NM_144672.4:c.618G>A
MANE Select
|
NP_653273.3:p.Glu206=
|
|
NM_001161683.2:c.381G>A
|
NP_001155155.1:p.Glu127=
|
|