NM_004364.5:c.1024T>G
MANE Select
|
NP_004355.2:p.Phe342Val
|
ENST00000498907.3:c.1024T>G
MANE Select
|
ENSP00000427514.1:p.Phe342Val
|
NM_001285829.1:c.667T>G
|
NP_001272758.1:p.Phe223Val
|
NM_001285829.2:c.667T>G
|
NP_001272758.1:p.Phe223Val
|
NM_001287424.1:c.1129T>G
|
NP_001274353.1:p.Phe377Val
|
NM_001287424.2:c.1129T>G
|
NP_001274353.1:p.Phe377Val
|
NM_001287435.1:c.982T>G
|
NP_001274364.1:p.Phe328Val
|
NM_001287435.2:c.982T>G
|
NP_001274364.1:p.Phe328Val
|
NM_004364.4:c.1024T>G
|
NP_004355.2:p.Phe342Val
|
ENST00000498907.2:c.1024T>G
|
ENSP00000427514.1:p.Phe342Val
|