ENST00000695651.1:n.795G>A
|
|
|
ENST00000695652.1:c.2324G>A
|
ENSP00000512083.1:p.Cys775Tyr
|
|
ENST00000695653.1:c.356G>A
|
ENSP00000512084.1:p.Cys119Tyr
|
|
ENST00000695654.1:c.1571G>A
|
ENSP00000512085.1:p.Cys524Tyr
|
|
ENST00000695655.1:c.1388G>A
|
ENSP00000512086.1:n.1388G>A
|
|
ENST00000695692.1:n.1811G>A
|
|
|
ENST00000245907.11:c.2447G>A
MANE Select
|
ENSP00000245907.4:p.Cys816Tyr
|
|
ENST00000245907.10:c.2447G>A
|
ENSP00000245907.4:p.Cys816Tyr
|
|
ENST00000602053.1:n.495G>A
|
|
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NM_000064.3:c.2447G>A
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NP_000055.2:p.Cys816Tyr
|
|
NM_000064.4:c.2447G>A
MANE Select
|
NP_000055.2:p.Cys816Tyr
|
|