ENST00000317447.9:c.1469A>G
|
ENSP00000320646.4:p.Glu490Gly
|
|
ENST00000614302.5:c.1469A>G
MANE Select
|
ENSP00000479130.1:p.Glu490Gly
|
|
ENST00000649953.1:c.1679A>G
|
ENSP00000497456.1:p.Glu560Gly
|
|
ENST00000317447.8:c.1469A>G
|
ENSP00000320646.4:p.Glu490Gly
|
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ENST00000378345.8:c.674A>G
|
ENSP00000367596.4:p.Glu225Gly
|
|
ENST00000406948.7:c.1469A>G
|
ENSP00000384627.3:p.Glu490Gly
|
|
ENST00000537116.5:n.595A>G
|
|
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ENST00000537155.1:n.209A>G
|
|
|
ENST00000542688.5:c.*213A>G
|
ENSP00000446281.1:n.*213A>G
|
|
ENST00000544543.5:c.674A>G
|
ENSP00000442781.1:p.Glu225Gly
|
|
ENST00000562204.1:n.442A>G
|
|
|
ENST00000614302.4:c.1469A>G
|
ENSP00000479130.1:p.Glu490Gly
|
|
NM_001127214.3:c.1469A>G
|
NP_001120686.1:p.Glu490Gly
|
|
NM_001243279.2:c.1469A>G
|
NP_001230208.1:p.Glu490Gly
|
|
NM_001284316.1:c.674A>G
|
NP_001271245.1:p.Glu225Gly
|
|
NM_174917.4:c.1469A>G
|
NP_777577.2:p.Glu490Gly
|
|
NR_045667.2:n.595A>G
|
|
|
NR_104293.1:n.1903A>G
|
|
|
XM_005256293.1:c.1469A>G
|
XP_005256350.1:p.Glu490Gly
|
|
XM_011522942.1:c.1469A>G
|
XP_011521244.1:p.Glu490Gly
|
|
XM_011522943.1:c.1469A>G
|
XP_011521245.1:p.Glu490Gly
|
|
XR_933239.1:n.1910A>G
|
|
|
XR_933240.1:n.1907A>G
|
|
|
XR_933241.1:n.1664A>G
|
|
|
NR_147928.1:n.1947A>G
|
|
|
NR_147929.1:n.1701A>G
|
|
|
XM_005256293.2:c.1469A>G
|
XP_005256350.1:p.Glu490Gly
|
|
XM_017023018.1:c.1469A>G
|
XP_016878507.1:p.Glu490Gly
|
|
XM_017023019.1:c.1469A>G
|
XP_016878508.1:p.Glu490Gly
|
|
XM_017023020.2:c.-3636A>G
|
XP_016878509.1:n.-3636A>G
|
|
XM_017023022.1:c.602A>G
|
XP_016878511.1:p.Glu201Gly
|
|
XM_024450186.1:c.674A>G
|
XP_024305954.1:p.Glu225Gly
|
|
XM_024450187.1:c.674A>G
|
XP_024305955.1:p.Glu225Gly
|
|
XR_001751864.2:n.1716A>G
|
|
|
XR_001751865.1:n.1663A>G
|
|
|
XR_933240.3:n.1906A>G
|
|
|
NM_001127214.4:c.1469A>G
|
NP_001120686.1:p.Glu490Gly
|
|
NM_001243279.3:c.1469A>G
MANE Select
|
NP_001230208.1:p.Glu490Gly
|
|
NM_001284316.2:c.674A>G
|
NP_001271245.1:p.Glu225Gly
|
|
NM_174917.5:c.1469A>G
|
NP_777577.2:p.Glu490Gly
|
|
NR_104293.2:n.1860A>G
|
|
|
NR_147928.2:n.1904A>G
|
|
|
NR_147929.2:n.1658A>G
|
|
|