ENST00000695651.1:n.2545T>C
|
|
|
ENST00000695653.1:c.2106T>C
|
ENSP00000512084.1:p.Thr702=
|
|
ENST00000695654.1:c.3222T>C
|
ENSP00000512085.1:p.Thr1074=
|
|
ENST00000695689.1:c.168T>C
|
ENSP00000512101.1:n.168T>C
|
|
ENST00000695690.1:n.388T>C
|
|
|
ENST00000695691.1:n.388T>C
|
|
|
ENST00000245907.11:c.4197T>C
MANE Select
|
ENSP00000245907.4:p.Thr1399=
|
|
ENST00000245907.10:c.4197T>C
|
ENSP00000245907.4:p.Thr1399=
|
|
ENST00000596548.1:c.318T>C
|
ENSP00000469744.1:p.Thr106=
|
|
ENST00000599899.5:n.1156T>C
|
|
|
ENST00000601008.1:c.242-4247T>C
|
ENSP00000471384.1:n.242-4247T>C
|
|
NM_000064.3:c.4197T>C
|
NP_000055.2:p.Thr1399=
|
|
NM_000064.4:c.4197T>C
MANE Select
|
NP_000055.2:p.Thr1399=
|
|