ENST00000253122.10:c.1160T>C
MANE Select
|
ENSP00000253122.5:p.Ile387Thr
|
|
ENST00000253122.9:c.1160T>C
|
ENSP00000253122.5:p.Ile387Thr
|
|
ENST00000413787.1:c.258-281T>C
|
ENSP00000400463.1:n.258-281T>C
|
|
ENST00000430077.6:c.815T>C
|
ENSP00000403041.2:p.Ile272Thr
|
|
ENST00000442457.1:c.214T>C
|
|
|
ENST00000457723.1:c.144T>C
|
ENSP00000394742.1:p.His48=
|
|
ENST00000467402.1:n.259T>C
|
|
|
ENST00000485324.1:n.1193T>C
|
|
|
NM_001142805.1:c.1130T>C
|
NP_001136277.1:p.Ile377Thr
|
|
NM_001142806.1:c.815T>C
|
NP_001136278.1:p.Ile272Thr
|
|
NM_005629.3:c.1160T>C
|
NP_005620.1:p.Ile387Thr
|
|
NM_005629.4:c.1160T>C
MANE Select
|
NP_005620.1:p.Ile387Thr
|
|
NM_001142805.2:c.1130T>C
|
NP_001136277.1:p.Ile377Thr
|
|