ENST00000695651.1:n.2060T>G
|
|
|
ENST00000695652.1:c.3589T>G
|
ENSP00000512083.1:p.Leu1197Val
|
|
ENST00000695653.1:c.1621T>G
|
ENSP00000512084.1:p.Leu541Val
|
|
ENST00000695654.1:c.2737T>G
|
ENSP00000512085.1:p.Leu913Val
|
|
ENST00000695655.1:c.2653T>G
|
ENSP00000512086.1:n.2653T>G
|
|
ENST00000695692.1:n.3076T>G
|
|
|
ENST00000245907.11:c.3712T>G
MANE Select
|
ENSP00000245907.4:p.Leu1238Val
|
|
ENST00000245907.10:c.3712T>G
|
ENSP00000245907.4:p.Leu1238Val
|
|
ENST00000596238.1:n.155T>G
|
|
|
ENST00000601008.1:c.241+524T>G
|
ENSP00000471384.1:n.241+524T>G
|
|
NM_000064.3:c.3712T>G
|
NP_000055.2:p.Leu1238Val
|
|
NM_000064.4:c.3712T>G
MANE Select
|
NP_000055.2:p.Leu1238Val
|
|