ENST00000695651.1:n.2293T>A
|
|
|
ENST00000695653.1:c.1854T>A
|
ENSP00000512084.1:p.Ser618=
|
|
ENST00000695654.1:c.2970T>A
|
ENSP00000512085.1:p.Ser990=
|
|
ENST00000695690.1:n.136T>A
|
|
|
ENST00000695691.1:n.136T>A
|
|
|
ENST00000245907.11:c.3945T>A
MANE Select
|
ENSP00000245907.4:p.Ser1315=
|
|
ENST00000245907.10:c.3945T>A
|
ENSP00000245907.4:p.Ser1315=
|
|
ENST00000596238.1:n.388T>A
|
|
|
ENST00000596548.1:c.27T>A
|
ENSP00000469744.1:p.Ser9=
|
|
ENST00000601008.1:c.241+1734T>A
|
ENSP00000471384.1:n.241+1734T>A
|
|
NM_000064.3:c.3945T>A
|
NP_000055.2:p.Ser1315=
|
|
NM_000064.4:c.3945T>A
MANE Select
|
NP_000055.2:p.Ser1315=
|
|