ENST00000695651.1:n.1002C>G
|
|
|
ENST00000695652.1:c.2531C>G
|
ENSP00000512083.1:p.Thr844Ser
|
|
ENST00000695653.1:c.563C>G
|
ENSP00000512084.1:p.Thr188Ser
|
|
ENST00000695654.1:c.1778C>G
|
ENSP00000512085.1:p.Thr593Ser
|
|
ENST00000695655.1:c.1595C>G
|
ENSP00000512086.1:n.1595C>G
|
|
ENST00000695692.1:n.2018C>G
|
|
|
ENST00000245907.11:c.2654C>G
MANE Select
|
ENSP00000245907.4:p.Thr885Ser
|
|
ENST00000245907.10:c.2654C>G
|
ENSP00000245907.4:p.Thr885Ser
|
|
ENST00000594005.1:n.230C>G
|
|
|
NM_000064.3:c.2654C>G
|
NP_000055.2:p.Thr885Ser
|
|
NM_000064.4:c.2654C>G
MANE Select
|
NP_000055.2:p.Thr885Ser
|
|