ENST00000225609.10:c.615G>A
MANE Select
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ENSP00000225609.5:p.Gln205=
|
|
ENST00000225609.9:c.615G>A
|
ENSP00000225609.5:p.Gln205=
|
|
ENST00000395844.8:c.583G>A
|
ENSP00000379185.3:p.Gly195Arg
|
|
ENST00000477745.5:n.613G>A
|
|
|
ENST00000488375.2:n.473G>A
|
|
|
ENST00000581006.5:c.426+17885G>A
|
ENSP00000462432.1:n.426+17885G>A
|
|
ENST00000596678.2:c.157G>A
|
ENSP00000470064.2:p.Gly53Arg
|
|
ENST00000613719.1:n.987+175G>A
|
|
|
NM_004278.3:c.615G>A
|
NP_004269.1:p.Gln205=
|
|
XR_243571.2:n.1613G>A
|
|
|
XM_017025349.1:c.*779G>A
|
XP_016880838.1:n.*779G>A
|
|
XM_017025350.1:c.*779G>A
|
XP_016880839.1:n.*779G>A
|
|
XM_017025351.1:c.*226G>A
|
XP_016880840.1:n.*226G>A
|
|
XM_017025352.1:c.615G>A
|
XP_016880841.1:p.Gln205=
|
|
XM_017025353.1:c.615G>A
|
XP_016880842.1:p.Gln205=
|
|
XM_017025354.1:c.583G>A
|
XP_016880843.1:p.Gly195Arg
|
|
XM_017025355.1:c.583G>A
|
XP_016880844.1:p.Gly195Arg
|
|
XM_017025356.1:c.*1092G>A
|
XP_016880845.1:n.*1092G>A
|
|
NM_004278.4:c.615G>A
MANE Select
|
NP_004269.1:p.Gln205=
|
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