ENST00000695651.1:n.2027C>T
|
|
|
ENST00000695652.1:c.3556C>T
|
ENSP00000512083.1:p.Leu1186Phe
|
|
ENST00000695653.1:c.1588C>T
|
ENSP00000512084.1:p.Leu530Phe
|
|
ENST00000695654.1:c.2704C>T
|
ENSP00000512085.1:p.Leu902Phe
|
|
ENST00000695655.1:c.2620C>T
|
ENSP00000512086.1:n.2620C>T
|
|
ENST00000695692.1:n.3043C>T
|
|
|
ENST00000245907.11:c.3679C>T
MANE Select
|
ENSP00000245907.4:p.Leu1227Phe
|
|
ENST00000245907.10:c.3679C>T
|
ENSP00000245907.4:p.Leu1227Phe
|
|
ENST00000596238.1:n.122C>T
|
|
|
ENST00000601008.1:c.241+491C>T
|
ENSP00000471384.1:n.241+491C>T
|
|
NM_000064.3:c.3679C>T
|
NP_000055.2:p.Leu1227Phe
|
|
NM_000064.4:c.3679C>T
MANE Select
|
NP_000055.2:p.Leu1227Phe
|
|