ENST00000695651.1:n.2821G>C
|
|
|
ENST00000695653.1:c.2382G>C
|
ENSP00000512084.1:p.Arg794=
|
|
ENST00000695654.1:c.3498G>C
|
ENSP00000512085.1:p.Arg1166=
|
|
ENST00000695689.1:c.444G>C
|
ENSP00000512101.1:n.444G>C
|
|
ENST00000695690.1:n.1538G>C
|
|
|
ENST00000695691.1:n.1334G>C
|
|
|
ENST00000245907.11:c.4473G>C
MANE Select
|
ENSP00000245907.4:p.Arg1491=
|
|
ENST00000245907.10:c.4473G>C
|
ENSP00000245907.4:p.Arg1491=
|
|
ENST00000599668.1:n.68G>C
|
|
|
ENST00000599899.5:n.1432G>C
|
|
|
ENST00000601008.1:c.242-1522G>C
|
ENSP00000471384.1:n.242-1522G>C
|
|
NM_000064.3:c.4473G>C
|
NP_000055.2:p.Arg1491=
|
|
NM_000064.4:c.4473G>C
MANE Select
|
NP_000055.2:p.Arg1491=
|
|