ENST00000695651.1:n.988G>C
|
|
|
ENST00000695652.1:c.2517G>C
|
ENSP00000512083.1:p.Arg839Ser
|
|
ENST00000695653.1:c.549G>C
|
ENSP00000512084.1:p.Arg183Ser
|
|
ENST00000695654.1:c.1764G>C
|
ENSP00000512085.1:p.Arg588Ser
|
|
ENST00000695655.1:c.1581G>C
|
ENSP00000512086.1:n.1581G>C
|
|
ENST00000695692.1:n.2004G>C
|
|
|
ENST00000245907.11:c.2640G>C
MANE Select
|
ENSP00000245907.4:p.Arg880Ser
|
|
ENST00000245907.10:c.2640G>C
|
ENSP00000245907.4:p.Arg880Ser
|
|
ENST00000594005.1:n.216G>C
|
|
|
NM_000064.3:c.2640G>C
|
NP_000055.2:p.Arg880Ser
|
|
NM_000064.4:c.2640G>C
MANE Select
|
NP_000055.2:p.Arg880Ser
|
|