ENST00000253122.10:c.1226T>C
MANE Select
|
ENSP00000253122.5:p.Met409Thr
|
|
ENST00000253122.9:c.1226T>C
|
ENSP00000253122.5:p.Met409Thr
|
|
ENST00000413787.1:c.258-215T>C
|
ENSP00000400463.1:n.258-215T>C
|
|
ENST00000430077.6:c.881T>C
|
ENSP00000403041.2:p.Met294Thr
|
|
ENST00000442457.1:c.280T>C
|
|
|
ENST00000457723.1:c.210T>C
|
ENSP00000394742.1:p.His70=
|
|
ENST00000485324.1:n.1259T>C
|
|
|
NM_001142805.1:c.1196T>C
|
NP_001136277.1:p.Met399Thr
|
|
NM_001142806.1:c.881T>C
|
NP_001136278.1:p.Met294Thr
|
|
NM_005629.3:c.1226T>C
|
NP_005620.1:p.Met409Thr
|
|
NM_005629.4:c.1226T>C
MANE Select
|
NP_005620.1:p.Met409Thr
|
|
NM_001142805.2:c.1196T>C
|
NP_001136277.1:p.Met399Thr
|
|