ENST00000399391.7:c.402T>G
|
ENSP00000382323.2:p.Thr134=
|
|
ENST00000399397.6:c.366T>G
MANE Select
|
ENSP00000382329.2:p.Thr122=
|
|
ENST00000399391.6:c.402T>G
|
ENSP00000382323.2:p.Thr134=
|
|
ENST00000399397.5:c.366T>G
|
ENSP00000382329.2:p.Thr122=
|
|
ENST00000428619.1:c.183T>G
|
ENSP00000399057.2:p.Thr61=
|
|
ENST00000498332.5:n.272T>G
|
|
|
NM_001277269.1:c.402T>G
|
NP_001264198.1:p.Thr134=
|
|
NM_001292063.1:c.366T>G
|
NP_001278992.1:p.Thr122=
|
|
NM_001277269.2:c.402T>G
|
NP_001264198.1:p.Thr134=
|
|
NM_001292063.2:c.366T>G
MANE Select
|
NP_001278992.1:p.Thr122=
|
|