ENST00000691183.1:c.*475A=
|
ENSP00000509954.1:n.*475A=
|
|
ENST00000378842.8:c.887A=
MANE Select
|
ENSP00000368119.4:p.Tyr296=
|
|
ENST00000378842.7:c.887A=
|
ENSP00000368119.3:p.Tyr296=
|
|
ENST00000450095.6:c.560A=
|
ENSP00000401956.2:p.Tyr187=
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|
ENST00000488412.2:n.143A=
|
|
|
ENST00000489643.6:n.967A=
|
|
|
ENST00000554550.5:c.*507A=
|
ENSP00000451435.1:n.*507A=
|
|
ENST00000554638.5:n.1359A=
|
|
|
ENST00000555020.5:n.1348A=
|
|
|
ENST00000555086.5:n.994A=
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|
|
ENST00000555754.1:n.335A=
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|
|
ENST00000556278.1:c.432+608A=
|
ENSP00000451792.1:n.432+608A=
|
|
ENST00000557706.5:n.1462A=
|
|
|
NM_000155.3:c.887A=
|
NP_000146.2:p.Tyr296=
|
|
NM_001258332.1:c.560A=
|
NP_001245261.1:p.Tyr187=
|
|
NM_000155.4:c.887A=
MANE Select
|
NP_000146.2:p.Tyr296=
|
|
NM_001258332.2:c.560A=
|
NP_001245261.1:p.Tyr187=
|
|