ENST00000695651.1:n.804A>T
|
|
|
ENST00000695652.1:c.2333A>T
|
ENSP00000512083.1:p.Asp778Val
|
|
ENST00000695653.1:c.365A>T
|
ENSP00000512084.1:p.Asp122Val
|
|
ENST00000695654.1:c.1580A>T
|
ENSP00000512085.1:p.Asp527Val
|
|
ENST00000695655.1:c.1397A>T
|
ENSP00000512086.1:n.1397A>T
|
|
ENST00000695692.1:n.1820A>T
|
|
|
ENST00000245907.11:c.2456A>T
MANE Select
|
ENSP00000245907.4:p.Asp819Val
|
|
ENST00000245907.10:c.2456A>T
|
ENSP00000245907.4:p.Asp819Val
|
|
ENST00000602053.1:n.504A>T
|
|
|
NM_000064.3:c.2456A>T
|
NP_000055.2:p.Asp819Val
|
|
NM_000064.4:c.2456A>T
MANE Select
|
NP_000055.2:p.Asp819Val
|
|