ENST00000695651.1:n.2813T>C
|
|
|
ENST00000695653.1:c.2374T>C
|
ENSP00000512084.1:p.Cys792Arg
|
|
ENST00000695654.1:c.3490T>C
|
ENSP00000512085.1:p.Cys1164Arg
|
|
ENST00000695689.1:c.436T>C
|
ENSP00000512101.1:n.436T>C
|
|
ENST00000695690.1:n.1530T>C
|
|
|
ENST00000695691.1:n.1326T>C
|
|
|
ENST00000245907.11:c.4465T>C
MANE Select
|
ENSP00000245907.4:p.Cys1489Arg
|
|
ENST00000245907.10:c.4465T>C
|
ENSP00000245907.4:p.Cys1489Arg
|
|
ENST00000599668.1:n.60T>C
|
|
|
ENST00000599899.5:n.1424T>C
|
|
|
ENST00000601008.1:c.242-1530T>C
|
ENSP00000471384.1:n.242-1530T>C
|
|
NM_000064.3:c.4465T>C
|
NP_000055.2:p.Cys1489Arg
|
|
NM_000064.4:c.4465T>C
MANE Select
|
NP_000055.2:p.Cys1489Arg
|
|