ENST00000695651.1:n.2061T>C
|
|
|
ENST00000695652.1:c.3590T>C
|
ENSP00000512083.1:p.Leu1197Ser
|
|
ENST00000695653.1:c.1622T>C
|
ENSP00000512084.1:p.Leu541Ser
|
|
ENST00000695654.1:c.2738T>C
|
ENSP00000512085.1:p.Leu913Ser
|
|
ENST00000695655.1:c.2654T>C
|
ENSP00000512086.1:n.2654T>C
|
|
ENST00000695692.1:n.3077T>C
|
|
|
ENST00000245907.11:c.3713T>C
MANE Select
|
ENSP00000245907.4:p.Leu1238Ser
|
|
ENST00000245907.10:c.3713T>C
|
ENSP00000245907.4:p.Leu1238Ser
|
|
ENST00000596238.1:n.156T>C
|
|
|
ENST00000601008.1:c.241+525T>C
|
ENSP00000471384.1:n.241+525T>C
|
|
NM_000064.3:c.3713T>C
|
NP_000055.2:p.Leu1238Ser
|
|
NM_000064.4:c.3713T>C
MANE Select
|
NP_000055.2:p.Leu1238Ser
|
|