ENST00000691183.1:c.*273A=
|
ENSP00000509954.1:n.*273A=
|
|
ENST00000378842.8:c.685A=
MANE Select
|
ENSP00000368119.4:p.Lys229=
|
|
ENST00000378842.7:c.685A=
|
ENSP00000368119.3:p.Lys229=
|
|
ENST00000450095.6:c.358A=
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ENSP00000401956.2:p.Lys120=
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|
ENST00000472111.5:n.941A=
|
|
|
ENST00000473506.6:c.*273A=
|
ENSP00000432839.2:n.*273A=
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|
ENST00000473529.5:n.844A=
|
|
|
ENST00000487381.5:n.1070A=
|
|
|
ENST00000489643.6:n.460A=
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|
|
ENST00000554085.5:c.*429A=
|
ENSP00000450419.1:n.*429A=
|
|
ENST00000554550.5:c.*305A=
|
ENSP00000451435.1:n.*305A=
|
|
ENST00000554638.5:n.1157A=
|
|
|
ENST00000555020.5:n.841A=
|
|
|
ENST00000555086.5:n.689A=
|
|
|
ENST00000555214.5:n.506A=
|
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|
ENST00000555754.1:n.30A=
|
|
|
ENST00000556244.1:c.672A=
|
|
|
ENST00000556278.1:c.430A=
|
ENSP00000451792.1:p.Lys144=
|
|
ENST00000556494.5:n.806A=
|
|
|
ENST00000557706.5:n.1247A=
|
|
|
NM_000155.3:c.685A=
|
NP_000146.2:p.Lys229=
|
|
NM_001258332.1:c.358A=
|
NP_001245261.1:p.Lys120=
|
|
NM_000155.4:c.685A=
MANE Select
|
NP_000146.2:p.Lys229=
|
|
NM_001258332.2:c.358A=
|
NP_001245261.1:p.Lys120=
|
|