ENST00000426263.10:c.958T>G
MANE Select
|
ENSP00000416293.2:p.Phe320Val
|
|
ENST00000674545.1:n.276T>G
|
|
|
ENST00000674765.1:c.958T>G
|
ENSP00000501811.1:p.Phe320Val
|
|
ENST00000675112.1:n.1259T>G
|
|
|
ENST00000676254.1:n.1407T>G
|
|
|
ENST00000426263.7:c.958T>G
|
ENSP00000416293.2:p.Phe320Val
|
|
ENST00000439722.2:c.837T>G
|
ENSP00000395521.2:n.837T>G
|
|
ENST00000475162.3:c.415+1402T>G
|
|
|
ENST00000630287.2:c.*273T>G
|
ENSP00000486694.1:n.*273T>G
|
|
NM_006516.2:c.958T>G
|
NP_006507.2:p.Phe320Val
|
|
NM_006516.3:c.958T>G
|
NP_006507.2:p.Phe320Val
|
|
NM_006516.4:c.958T>G
MANE Select
|
NP_006507.2:p.Phe320Val
|
|