ENST00000695651.1:n.2091T>C
|
|
|
ENST00000695652.1:c.3620T>C
|
ENSP00000512083.1:p.Phe1207Ser
|
|
ENST00000695653.1:c.1652T>C
|
ENSP00000512084.1:p.Phe551Ser
|
|
ENST00000695654.1:c.2768T>C
|
ENSP00000512085.1:p.Phe923Ser
|
|
ENST00000695655.1:c.2684T>C
|
ENSP00000512086.1:n.2684T>C
|
|
ENST00000695692.1:n.3107T>C
|
|
|
ENST00000245907.11:c.3743T>C
MANE Select
|
ENSP00000245907.4:p.Phe1248Ser
|
|
ENST00000245907.10:c.3743T>C
|
ENSP00000245907.4:p.Phe1248Ser
|
|
ENST00000596238.1:n.186T>C
|
|
|
ENST00000601008.1:c.241+555T>C
|
ENSP00000471384.1:n.241+555T>C
|
|
NM_000064.3:c.3743T>C
|
NP_000055.2:p.Phe1248Ser
|
|
NM_000064.4:c.3743T>C
MANE Select
|
NP_000055.2:p.Phe1248Ser
|
|