ENST00000369409.9:c.422C>A
|
ENSP00000358417.5:p.Thr141Lys
|
|
ENST00000462324.2:n.505C>A
|
|
|
ENST00000641023.2:c.422C>A
MANE Select
|
ENSP00000493175.1:p.Thr141Lys
|
|
ENST00000641074.1:c.422C>A
|
ENSP00000493446.1:p.Thr141Lys
|
|
ENST00000641115.1:c.422C>A
|
ENSP00000493264.1:p.Thr141Lys
|
|
ENST00000641213.1:c.*75C>A
|
ENSP00000493079.1:n.*75C>A
|
|
ENST00000641247.1:c.*141C>A
|
ENSP00000492955.1:n.*141C>A
|
|
ENST00000641272.1:c.356C>A
|
ENSP00000493432.1:p.Thr119Lys
|
|
ENST00000641314.1:n.407C>A
|
|
|
ENST00000641371.1:c.336C>A
|
ENSP00000493305.1:p.Asn112Lys
|
|
ENST00000641375.1:c.*258C>A
|
ENSP00000493089.1:n.*258C>A
|
|
ENST00000641491.1:c.*75C>A
|
ENSP00000493187.1:n.*75C>A
|
|
ENST00000641570.1:c.*141C>A
|
ENSP00000493213.1:n.*141C>A
|
|
ENST00000641573.1:n.510C>A
|
|
|
ENST00000641587.1:c.*133C>A
|
ENSP00000493453.1:n.*133C>A
|
|
ENST00000641597.1:c.422C>A
|
ENSP00000493382.1:p.Thr141Lys
|
|
ENST00000641711.1:n.646C>A
|
|
|
ENST00000641756.1:c.*166C>A
|
ENSP00000493147.1:n.*166C>A
|
|
ENST00000641811.1:c.178C>A
|
|
|
ENST00000641847.1:n.281C>A
|
|
|
ENST00000641891.1:c.*248C>A
|
ENSP00000493288.1:n.*248C>A
|
|
ENST00000641927.1:n.362C>A
|
|
|
ENST00000641947.1:c.422C>A
|
ENSP00000492994.1:p.Thr141Lys
|
|
ENST00000642021.1:n.544C>A
|
|
|
ENST00000642041.1:c.*461C>A
|
ENSP00000493415.1:n.*461C>A
|
|
ENST00000369407.3:c.320C>A
|
ENSP00000358415.3:p.Thr107Lys
|
|
ENST00000369409.8:c.422C>A
|
ENSP00000358417.4:p.Thr141Lys
|
|
ENST00000462324.1:n.690C>A
|
|
|
ENST00000493622.5:n.611C>A
|
|
|
NM_006623.3:c.422C>A
|
NP_006614.2:p.Thr141Lys
|
|
XM_011541226.1:c.644C>A
|
XP_011539528.1:p.Thr215Lys
|
|
XM_011541227.1:c.566C>A
|
XP_011539529.1:p.Thr189Lys
|
|
XM_011541228.1:c.533C>A
|
XP_011539530.1:p.Thr178Lys
|
|
XM_011541229.1:c.359C>A
|
XP_011539531.1:p.Thr120Lys
|
|
XM_011541230.1:c.137C>A
|
XP_011539532.1:p.Thr46Lys
|
|
XM_011541231.1:c.128C>A
|
XP_011539533.1:p.Thr43Lys
|
|
XM_011541226.2:c.644C>A
|
XP_011539528.1:p.Thr215Lys
|
|
XM_011541227.2:c.566C>A
|
XP_011539529.1:p.Thr189Lys
|
|
XM_011541228.2:c.533C>A
|
XP_011539530.1:p.Thr178Lys
|
|
XM_011541231.2:c.128C>A
|
XP_011539533.1:p.Thr43Lys
|
|
XM_024446338.1:c.533C>A
|
XP_024302106.1:p.Thr178Lys
|
|
NM_006623.4:c.422C>A
MANE Select
|
NP_006614.2:p.Thr141Lys
|
|