ENST00000650793.2:n.567C>G
|
|
|
ENST00000697612.1:n.1245C>G
|
|
|
ENST00000374881.3:c.376C>G
|
ENSP00000364015.2:p.Leu126Val
|
|
ENST00000374882.8:c.388C>G
MANE Select
|
ENSP00000364016.4:p.Leu130Val
|
|
ENST00000650411.1:n.1709C>G
|
|
|
ENST00000650793.1:n.567C>G
|
|
|
ENST00000374881.2:c.376C>G
|
ENSP00000364015.2:p.Leu126Val
|
|
ENST00000374882.7:c.388C>G
|
ENSP00000364016.3:p.Leu130Val
|
|
ENST00000395339.7:c.316C>G
|
ENSP00000378748.3:p.Leu106Val
|
|
ENST00000484003.1:n.772C>G
|
|
|
NM_004159.4:c.376C>G
|
NP_004150.1:p.Leu126Val
|
|
NM_148919.3:c.388C>G
|
NP_683720.2:p.Leu130Val
|
|
NM_148919.4:c.388C>G
MANE Select
|
NP_683720.2:p.Leu130Val
|
|
NM_004159.5:c.376C>G
|
NP_004150.1:p.Leu126Val
|
|