|
ENST00000700029.2:c.735G>A
|
ENSP00000514759.2:p.Gln245=
|
|
|
ENST00000710265.1:c.735G>A
|
ENSP00000518161.1:p.Gln245=
|
|
|
ENST00000472832.3:c.735G>A
|
ENSP00000483066.2:p.Gln245=
|
|
|
ENST00000688158.2:n.1470G>A
|
|
|
|
ENST00000688922.2:c.*565G>A
|
ENSP00000508742.2:n.*565G>A
|
|
|
ENST00000700021.1:c.690G>A
|
ENSP00000514757.1:p.Gln230=
|
|
|
ENST00000700022.1:c.*74G>A
|
ENSP00000514758.1:n.*74G>A
|
|
|
ENST00000700023.1:n.1893G>A
|
|
|
|
ENST00000700024.1:n.2127G>A
|
|
|
|
ENST00000700025.1:n.1504G>A
|
|
|
|
ENST00000700026.1:n.372G>A
|
|
|
|
ENST00000700029.1:c.569G>A
|
|
|
|
ENST00000706954.1:c.735G>A
|
ENSP00000516674.1:p.Gln245=
|
|
|
ENST00000706955.1:c.*770G>A
|
ENSP00000516675.1:n.*770G>A
|
|
|
ENST00000686459.1:c.*321G>A
|
ENSP00000508909.1:n.*321G>A
|
|
|
ENST00000688158.1:c.*846G>A
|
ENSP00000509254.1:n.*846G>A
|
|
|
ENST00000688308.1:c.735G>A
|
ENSP00000508752.1:p.Gln245=
|
|
|
ENST00000688922.1:c.656G>A
|
|
|
|
ENST00000693560.1:c.1254G>A
|
ENSP00000509861.1:p.Gln418=
|
|
|
ENST00000371953.8:c.735G>A
MANE Select
|
ENSP00000361021.3:p.Gln245=
|
|
|
ENST00000371953.7:c.735G>A
|
ENSP00000361021.3:p.Gln245=
|
|
|
ENST00000472832.2:c.162G>A
|
ENSP00000483066.1:p.Gln54=
|
|
|
NM_000314.5:c.735G>A
|
NP_000305.3:p.Gln245=
|
|
|
NM_000314.6:c.735G>A
|
NP_000305.3:p.Gln245=
|
|
|
NM_001304717.2:c.1254G>A
|
NP_001291646.2:p.Gln418=
|
|
|
NM_001304718.1:c.144G>A
|
NP_001291647.1:p.Gln48=
|
|
|
XM_006717926.2:c.690G>A
|
XP_006717989.1:p.Gln230=
|
|
|
XM_011539981.1:c.735G>A
|
XP_011538283.1:p.Gln245=
|
|
|
XM_011539982.1:c.639G>A
|
XP_011538284.1:p.Gln213=
|
|
|
XR_945791.1:n.1305G>A
|
|
|
|
NM_000314.7:c.735G>A
|
NP_000305.3:p.Gln245=
|
|
|
NM_001304717.5:c.1254G>A
|
NP_001291646.4:p.Gln418=
|
|
|
NM_001304718.2:c.144G>A
|
NP_001291647.1:p.Gln48=
|
|
|
NM_000314.8:c.735G>A
MANE Select
|
NP_000305.3:p.Gln245=
|
|
