ENST00000695651.1:n.971C>G
|
|
|
ENST00000695652.1:c.2500C>G
|
ENSP00000512083.1:p.Leu834Val
|
|
ENST00000695653.1:c.532C>G
|
ENSP00000512084.1:p.Leu178Val
|
|
ENST00000695654.1:c.1747C>G
|
ENSP00000512085.1:p.Leu583Val
|
|
ENST00000695655.1:c.1564C>G
|
ENSP00000512086.1:n.1564C>G
|
|
ENST00000695692.1:n.1987C>G
|
|
|
ENST00000245907.11:c.2623C>G
MANE Select
|
ENSP00000245907.4:p.Leu875Val
|
|
ENST00000245907.10:c.2623C>G
|
ENSP00000245907.4:p.Leu875Val
|
|
ENST00000594005.1:n.199C>G
|
|
|
NM_000064.3:c.2623C>G
|
NP_000055.2:p.Leu875Val
|
|
NM_000064.4:c.2623C>G
MANE Select
|
NP_000055.2:p.Leu875Val
|
|