ENST00000253122.10:c.1182G>C
MANE Select
|
ENSP00000253122.5:p.Thr394=
|
|
ENST00000253122.9:c.1182G>C
|
ENSP00000253122.5:p.Thr394=
|
|
ENST00000413787.1:c.258-259G>C
|
ENSP00000400463.1:n.258-259G>C
|
|
ENST00000430077.6:c.837G>C
|
ENSP00000403041.2:p.Thr279=
|
|
ENST00000442457.1:c.236G>C
|
|
|
ENST00000457723.1:c.166G>C
|
ENSP00000394742.1:p.Ala56Pro
|
|
ENST00000467402.1:n.281G>C
|
|
|
ENST00000485324.1:n.1215G>C
|
|
|
NM_001142805.1:c.1152G>C
|
NP_001136277.1:p.Thr384=
|
|
NM_001142806.1:c.837G>C
|
NP_001136278.1:p.Thr279=
|
|
NM_005629.3:c.1182G>C
|
NP_005620.1:p.Thr394=
|
|
NM_005629.4:c.1182G>C
MANE Select
|
NP_005620.1:p.Thr394=
|
|
NM_001142805.2:c.1152G>C
|
NP_001136277.1:p.Thr384=
|
|