ENST00000695651.1:n.1801G>C
|
|
|
ENST00000695652.1:c.3330G>C
|
ENSP00000512083.1:p.Leu1110=
|
|
ENST00000695653.1:c.1362G>C
|
ENSP00000512084.1:p.Leu454=
|
|
ENST00000695654.1:c.2514+2259G>C
|
ENSP00000512085.1:n.2514+2259G>C
|
|
ENST00000695655.1:c.2394G>C
|
ENSP00000512086.1:n.2394G>C
|
|
ENST00000695692.1:n.2817G>C
|
|
|
ENST00000245907.11:c.3453G>C
MANE Select
|
ENSP00000245907.4:p.Leu1151=
|
|
ENST00000245907.10:c.3453G>C
|
ENSP00000245907.4:p.Leu1151=
|
|
ENST00000598805.2:n.223G>C
|
|
|
ENST00000601008.1:c.48G>C
|
ENSP00000471384.1:p.Leu16=
|
|
NM_000064.3:c.3453G>C
|
NP_000055.2:p.Leu1151=
|
|
NM_000064.4:c.3453G>C
MANE Select
|
NP_000055.2:p.Leu1151=
|
|