ENST00000695651.1:n.1030G>T
|
|
|
ENST00000695652.1:c.2559G>T
|
ENSP00000512083.1:p.Leu853Phe
|
|
ENST00000695653.1:c.591G>T
|
ENSP00000512084.1:p.Leu197Phe
|
|
ENST00000695654.1:c.1806G>T
|
ENSP00000512085.1:p.Leu602Phe
|
|
ENST00000695655.1:c.1623G>T
|
ENSP00000512086.1:n.1623G>T
|
|
ENST00000695692.1:n.2046G>T
|
|
|
ENST00000245907.11:c.2682G>T
MANE Select
|
ENSP00000245907.4:p.Leu894Phe
|
|
ENST00000245907.10:c.2682G>T
|
ENSP00000245907.4:p.Leu894Phe
|
|
ENST00000594005.1:n.258G>T
|
|
|
NM_000064.3:c.2682G>T
|
NP_000055.2:p.Leu894Phe
|
|
NM_000064.4:c.2682G>T
MANE Select
|
NP_000055.2:p.Leu894Phe
|
|