ENST00000691183.1:c.*231G>A
|
ENSP00000509954.1:n.*231G>A
|
|
ENST00000378842.8:c.643G>A
MANE Select
|
ENSP00000368119.4:p.Glu215Lys
|
|
ENST00000378842.7:c.643G>A
|
ENSP00000368119.3:p.Glu215Lys
|
|
ENST00000450095.6:c.316G>A
|
ENSP00000401956.2:p.Glu106Lys
|
|
ENST00000472111.5:n.899G>A
|
|
|
ENST00000473506.6:c.*231G>A
|
ENSP00000432839.2:n.*231G>A
|
|
ENST00000473529.5:n.802G>A
|
|
|
ENST00000487381.5:n.1028G>A
|
|
|
ENST00000489643.6:n.418G>A
|
|
|
ENST00000554085.5:c.*387G>A
|
ENSP00000450419.1:n.*387G>A
|
|
ENST00000554550.5:c.*263G>A
|
ENSP00000451435.1:n.*263G>A
|
|
ENST00000554638.5:n.1115G>A
|
|
|
ENST00000555020.5:n.799G>A
|
|
|
ENST00000555086.5:n.647G>A
|
|
|
ENST00000555214.5:n.464G>A
|
|
|
ENST00000556244.1:c.630G>A
|
|
|
ENST00000556278.1:c.388G>A
|
ENSP00000451792.1:p.Glu130Lys
|
|
ENST00000556494.5:n.764G>A
|
|
|
ENST00000557706.5:n.1205G>A
|
|
|
NM_000155.3:c.643G>A
|
NP_000146.2:p.Glu215Lys
|
|
NM_001258332.1:c.316G>A
|
NP_001245261.1:p.Glu106Lys
|
|
NM_000155.4:c.643G>A
MANE Select
|
NP_000146.2:p.Glu215Lys
|
|
NM_001258332.2:c.316G>A
|
NP_001245261.1:p.Glu106Lys
|
|