ENST00000426263.10:c.1183T>G
MANE Select
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ENSP00000416293.2:p.Phe395Val
|
|
ENST00000674545.1:n.1800T>G
|
|
|
ENST00000674765.1:c.1030-843T>G
|
ENSP00000501811.1:n.1030-843T>G
|
|
ENST00000675112.1:n.1484T>G
|
|
|
ENST00000676254.1:n.1632T>G
|
|
|
ENST00000426263.7:c.1183T>G
|
ENSP00000416293.2:p.Phe395Val
|
|
ENST00000475162.3:c.416-722T>G
|
|
|
ENST00000630287.2:c.*498T>G
|
ENSP00000486694.1:n.*498T>G
|
|
NM_006516.2:c.1183T>G
|
NP_006507.2:p.Phe395Val
|
|
NM_006516.3:c.1183T>G
|
NP_006507.2:p.Phe395Val
|
|
NM_006516.4:c.1183T>G
MANE Select
|
NP_006507.2:p.Phe395Val
|
|