ENST00000695651.1:n.1126G>T
|
|
|
ENST00000695652.1:c.2655G>T
|
ENSP00000512083.1:p.Arg885Ser
|
|
ENST00000695653.1:c.687G>T
|
ENSP00000512084.1:p.Arg229Ser
|
|
ENST00000695654.1:c.1902G>T
|
ENSP00000512085.1:p.Arg634Ser
|
|
ENST00000695655.1:c.1719G>T
|
ENSP00000512086.1:n.1719G>T
|
|
ENST00000695692.1:n.2142G>T
|
|
|
ENST00000245907.11:c.2778G>T
MANE Select
|
ENSP00000245907.4:p.Arg926Ser
|
|
ENST00000245907.10:c.2778G>T
|
ENSP00000245907.4:p.Arg926Ser
|
|
ENST00000594005.1:n.354G>T
|
|
|
NM_000064.3:c.2778G>T
|
NP_000055.2:p.Arg926Ser
|
|
NM_000064.4:c.2778G>T
MANE Select
|
NP_000055.2:p.Arg926Ser
|
|