ENST00000695651.1:n.2005C>A
|
|
|
ENST00000695652.1:c.3534C>A
|
ENSP00000512083.1:p.Arg1178=
|
|
ENST00000695653.1:c.1566C>A
|
ENSP00000512084.1:p.Arg522=
|
|
ENST00000695654.1:c.2682C>A
|
ENSP00000512085.1:p.Arg894=
|
|
ENST00000695655.1:c.2598C>A
|
ENSP00000512086.1:n.2598C>A
|
|
ENST00000695692.1:n.3021C>A
|
|
|
ENST00000245907.11:c.3657C>A
MANE Select
|
ENSP00000245907.4:p.Arg1219=
|
|
ENST00000245907.10:c.3657C>A
|
ENSP00000245907.4:p.Arg1219=
|
|
ENST00000596238.1:n.100C>A
|
|
|
ENST00000601008.1:c.241+469C>A
|
ENSP00000471384.1:n.241+469C>A
|
|
NM_000064.3:c.3657C>A
|
NP_000055.2:p.Arg1219=
|
|
NM_000064.4:c.3657C>A
MANE Select
|
NP_000055.2:p.Arg1219=
|
|