ENST00000695651.1:n.1007A>G
|
|
|
ENST00000695652.1:c.2536A>G
|
ENSP00000512083.1:p.Thr846Ala
|
|
ENST00000695653.1:c.568A>G
|
ENSP00000512084.1:p.Thr190Ala
|
|
ENST00000695654.1:c.1783A>G
|
ENSP00000512085.1:p.Thr595Ala
|
|
ENST00000695655.1:c.1600A>G
|
ENSP00000512086.1:n.1600A>G
|
|
ENST00000695692.1:n.2023A>G
|
|
|
ENST00000245907.11:c.2659A>G
MANE Select
|
ENSP00000245907.4:p.Thr887Ala
|
|
ENST00000245907.10:c.2659A>G
|
ENSP00000245907.4:p.Thr887Ala
|
|
ENST00000594005.1:n.235A>G
|
|
|
NM_000064.3:c.2659A>G
|
NP_000055.2:p.Thr887Ala
|
|
NM_000064.4:c.2659A>G
MANE Select
|
NP_000055.2:p.Thr887Ala
|
|