ENST00000253122.10:c.1156T>G
MANE Select
|
ENSP00000253122.5:p.Phe386Val
|
|
ENST00000253122.9:c.1156T>G
|
ENSP00000253122.5:p.Phe386Val
|
|
ENST00000413787.1:c.258-285T>G
|
ENSP00000400463.1:n.258-285T>G
|
|
ENST00000430077.6:c.811T>G
|
ENSP00000403041.2:p.Phe271Val
|
|
ENST00000442457.1:c.210T>G
|
|
|
ENST00000457723.1:c.140T>G
|
ENSP00000394742.1:p.Leu47Arg
|
|
ENST00000467402.1:n.255T>G
|
|
|
ENST00000485324.1:n.1189T>G
|
|
|
NM_001142805.1:c.1126T>G
|
NP_001136277.1:p.Phe376Val
|
|
NM_001142806.1:c.811T>G
|
NP_001136278.1:p.Phe271Val
|
|
NM_005629.3:c.1156T>G
|
NP_005620.1:p.Phe386Val
|
|
NM_005629.4:c.1156T>G
MANE Select
|
NP_005620.1:p.Phe386Val
|
|
NM_001142805.2:c.1126T>G
|
NP_001136277.1:p.Phe376Val
|
|