ENST00000695651.1:n.2062G>T
|
|
|
ENST00000695652.1:c.3591G>T
|
ENSP00000512083.1:p.Leu1197Phe
|
|
ENST00000695653.1:c.1623G>T
|
ENSP00000512084.1:p.Leu541Phe
|
|
ENST00000695654.1:c.2739G>T
|
ENSP00000512085.1:p.Leu913Phe
|
|
ENST00000695655.1:c.2655G>T
|
ENSP00000512086.1:n.2655G>T
|
|
ENST00000695692.1:n.3078G>T
|
|
|
ENST00000245907.11:c.3714G>T
MANE Select
|
ENSP00000245907.4:p.Leu1238Phe
|
|
ENST00000245907.10:c.3714G>T
|
ENSP00000245907.4:p.Leu1238Phe
|
|
ENST00000596238.1:n.157G>T
|
|
|
ENST00000601008.1:c.241+526G>T
|
ENSP00000471384.1:n.241+526G>T
|
|
NM_000064.3:c.3714G>T
|
NP_000055.2:p.Leu1238Phe
|
|
NM_000064.4:c.3714G>T
MANE Select
|
NP_000055.2:p.Leu1238Phe
|
|