ENST00000695651.1:n.2311A>T
|
|
|
ENST00000695653.1:c.1872A>T
|
ENSP00000512084.1:p.Ser624=
|
|
ENST00000695654.1:c.2988A>T
|
ENSP00000512085.1:p.Ser996=
|
|
ENST00000695690.1:n.154A>T
|
|
|
ENST00000695691.1:n.154A>T
|
|
|
ENST00000245907.11:c.3963A>T
MANE Select
|
ENSP00000245907.4:p.Ser1321=
|
|
ENST00000245907.10:c.3963A>T
|
ENSP00000245907.4:p.Ser1321=
|
|
ENST00000596238.1:n.406A>T
|
|
|
ENST00000596548.1:c.45A>T
|
ENSP00000469744.1:p.Ser15=
|
|
ENST00000601008.1:c.241+1752A>T
|
ENSP00000471384.1:n.241+1752A>T
|
|
NM_000064.3:c.3963A>T
|
NP_000055.2:p.Ser1321=
|
|
NM_000064.4:c.3963A>T
MANE Select
|
NP_000055.2:p.Ser1321=
|
|