ENST00000691183.1:c.*272G>A
|
ENSP00000509954.1:n.*272G>A
|
|
ENST00000378842.8:c.684G>A
MANE Select
|
ENSP00000368119.4:p.Arg228=
|
|
ENST00000378842.7:c.684G>A
|
ENSP00000368119.3:p.Arg228=
|
|
ENST00000450095.6:c.357G>A
|
ENSP00000401956.2:p.Arg119=
|
|
ENST00000472111.5:n.940G>A
|
|
|
ENST00000473506.6:c.*272G>A
|
ENSP00000432839.2:n.*272G>A
|
|
ENST00000473529.5:n.843G>A
|
|
|
ENST00000487381.5:n.1069G>A
|
|
|
ENST00000489643.6:n.459G>A
|
|
|
ENST00000554085.5:c.*428G>A
|
ENSP00000450419.1:n.*428G>A
|
|
ENST00000554550.5:c.*304G>A
|
ENSP00000451435.1:n.*304G>A
|
|
ENST00000554638.5:n.1156G>A
|
|
|
ENST00000555020.5:n.840G>A
|
|
|
ENST00000555086.5:n.688G>A
|
|
|
ENST00000555214.5:n.505G>A
|
|
|
ENST00000555754.1:n.29G>A
|
|
|
ENST00000556244.1:c.671G>A
|
|
|
ENST00000556278.1:c.429G>A
|
ENSP00000451792.1:p.Arg143=
|
|
ENST00000556494.5:n.805G>A
|
|
|
ENST00000557706.5:n.1246G>A
|
|
|
NM_000155.3:c.684G>A
|
NP_000146.2:p.Arg228=
|
|
NM_001258332.1:c.357G>A
|
NP_001245261.1:p.Arg119=
|
|
NM_000155.4:c.684G>A
MANE Select
|
NP_000146.2:p.Arg228=
|
|
NM_001258332.2:c.357G>A
|
NP_001245261.1:p.Arg119=
|
|