ENST00000542664.4:c.456T>C
MANE Select
|
ENSP00000437737.1:p.Ile152=
|
|
ENST00000543956.5:c.-34T>C
|
ENSP00000441861.2:n.-34T>C
|
|
ENST00000378688.8:c.456T>C
|
ENSP00000367959.3:p.Ile152=
|
|
ENST00000542664.3:c.456T>C
|
ENSP00000437737.1:p.Ile152=
|
|
ENST00000543956.4:c.204T>C
|
ENSP00000441861.1:p.Ile68=
|
|
NM_000621.4:c.456T>C
|
NP_000612.1:p.Ile152=
|
|
NM_001165947.2:c.204T>C
|
NP_001159419.1:p.Ile68=
|
|
NM_000621.5:c.456T>C
MANE Select
|
NP_000612.1:p.Ile152=
|
|
NM_001165947.5:c.-34T>C
|
NP_001159419.2:n.-34T>C
|
|
NM_001378924.1:c.456T>C
|
NP_001365853.1:p.Ile152=
|
|