ENST00000695651.1:n.862T>C
|
|
|
ENST00000695652.1:c.2391T>C
|
ENSP00000512083.1:p.Ser797=
|
|
ENST00000695653.1:c.423T>C
|
ENSP00000512084.1:p.Ser141=
|
|
ENST00000695654.1:c.1638T>C
|
ENSP00000512085.1:p.Ser546=
|
|
ENST00000695655.1:c.1455T>C
|
ENSP00000512086.1:n.1455T>C
|
|
ENST00000695692.1:n.1878T>C
|
|
|
ENST00000245907.11:c.2514T>C
MANE Select
|
ENSP00000245907.4:p.Ser838=
|
|
ENST00000245907.10:c.2514T>C
|
ENSP00000245907.4:p.Ser838=
|
|
ENST00000602053.1:n.562T>C
|
|
|
NM_000064.3:c.2514T>C
|
NP_000055.2:p.Ser838=
|
|
NM_000064.4:c.2514T>C
MANE Select
|
NP_000055.2:p.Ser838=
|
|