ENST00000695651.1:n.969G>C
|
|
|
ENST00000695652.1:c.2498G>C
|
ENSP00000512083.1:p.Ser833Thr
|
|
ENST00000695653.1:c.530G>C
|
ENSP00000512084.1:p.Ser177Thr
|
|
ENST00000695654.1:c.1745G>C
|
ENSP00000512085.1:p.Ser582Thr
|
|
ENST00000695655.1:c.1562G>C
|
ENSP00000512086.1:n.1562G>C
|
|
ENST00000695692.1:n.1985G>C
|
|
|
ENST00000245907.11:c.2621G>C
MANE Select
|
ENSP00000245907.4:p.Ser874Thr
|
|
ENST00000245907.10:c.2621G>C
|
ENSP00000245907.4:p.Ser874Thr
|
|
ENST00000594005.1:n.197G>C
|
|
|
NM_000064.3:c.2621G>C
|
NP_000055.2:p.Ser874Thr
|
|
NM_000064.4:c.2621G>C
MANE Select
|
NP_000055.2:p.Ser874Thr
|
|