ENST00000691183.1:c.*317C>A
|
ENSP00000509954.1:n.*317C>A
|
|
ENST00000378842.8:c.729C>A
MANE Select
|
ENSP00000368119.4:p.Val243=
|
|
ENST00000378842.7:c.729C>A
|
ENSP00000368119.3:p.Val243=
|
|
ENST00000450095.6:c.402C>A
|
ENSP00000401956.2:p.Val134=
|
|
ENST00000473506.6:c.*317C>A
|
ENSP00000432839.2:n.*317C>A
|
|
ENST00000473529.5:n.888C>A
|
|
|
ENST00000487381.5:n.1419C>A
|
|
|
ENST00000489643.6:n.809C>A
|
|
|
ENST00000554085.5:c.*473C>A
|
ENSP00000450419.1:n.*473C>A
|
|
ENST00000554550.5:c.*349C>A
|
ENSP00000451435.1:n.*349C>A
|
|
ENST00000554638.5:n.1201C>A
|
|
|
ENST00000555020.5:n.1190C>A
|
|
|
ENST00000555086.5:n.733C>A
|
|
|
ENST00000555754.1:n.74C>A
|
|
|
ENST00000556244.1:c.716C>A
|
|
|
ENST00000556278.1:c.432+347C>A
|
ENSP00000451792.1:n.432+347C>A
|
|
ENST00000557706.5:n.1291C>A
|
|
|
NM_000155.3:c.729C>A
|
NP_000146.2:p.Val243=
|
|
NM_001258332.1:c.402C>A
|
NP_001245261.1:p.Val134=
|
|
NM_000155.4:c.729C>A
MANE Select
|
NP_000146.2:p.Val243=
|
|
NM_001258332.2:c.402C>A
|
NP_001245261.1:p.Val134=
|
|