ENST00000695651.1:n.2086T>C
|
|
|
ENST00000695652.1:c.3615T>C
|
ENSP00000512083.1:p.Phe1205=
|
|
ENST00000695653.1:c.1647T>C
|
ENSP00000512084.1:p.Phe549=
|
|
ENST00000695654.1:c.2763T>C
|
ENSP00000512085.1:p.Phe921=
|
|
ENST00000695655.1:c.2679T>C
|
ENSP00000512086.1:n.2679T>C
|
|
ENST00000695692.1:n.3102T>C
|
|
|
ENST00000245907.11:c.3738T>C
MANE Select
|
ENSP00000245907.4:p.Phe1246=
|
|
ENST00000245907.10:c.3738T>C
|
ENSP00000245907.4:p.Phe1246=
|
|
ENST00000596238.1:n.181T>C
|
|
|
ENST00000601008.1:c.241+550T>C
|
ENSP00000471384.1:n.241+550T>C
|
|
NM_000064.3:c.3738T>C
|
NP_000055.2:p.Phe1246=
|
|
NM_000064.4:c.3738T>C
MANE Select
|
NP_000055.2:p.Phe1246=
|
|