ENST00000692585.1:c.305A>G
|
ENSP00000509200.1:p.Glu102Gly
|
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ENST00000294309.8:c.1448A>G
MANE Select
|
ENSP00000294309.3:p.Glu483Gly
|
|
ENST00000635811.1:c.1448A>G
|
ENSP00000490341.1:p.Glu483Gly
|
|
ENST00000637084.1:c.305A>G
|
ENSP00000490615.1:p.Glu102Gly
|
|
ENST00000637342.1:c.1448A>G
|
ENSP00000490171.1:p.Glu483Gly
|
|
ENST00000637504.1:c.1448A>G
|
ENSP00000489759.1:p.Glu483Gly
|
|
ENST00000294309.7:c.1448A>G
|
ENSP00000294309.3:p.Glu483Gly
|
|
ENST00000442692.2:n.1041A>G
|
|
|
ENST00000535009.5:n.1257A>G
|
|
|
ENST00000542467.1:c.1448A>G
|
ENSP00000445551.1:p.Glu483Gly
|
|
NM_139075.3:c.1448A>G
|
NP_620714.2:p.Glu483Gly
|
|
XM_005273824.2:c.1445A>G
|
XP_005273881.1:p.Glu482Gly
|
|
XM_005273826.2:c.1193A>G
|
XP_005273883.1:p.Glu398Gly
|
|
XM_005273827.2:c.1448A>G
|
XP_005273884.1:p.Glu483Gly
|
|
XM_005273828.2:c.1448A>G
|
XP_005273885.1:p.Glu483Gly
|
|
XM_005273830.2:c.755A>G
|
XP_005273887.1:p.Glu252Gly
|
|
XM_005273831.2:c.755A>G
|
XP_005273888.1:p.Glu252Gly
|
|
XM_005273832.2:c.725A>G
|
XP_005273889.1:p.Glu242Gly
|
|
XM_006718453.2:c.1448A>G
|
XP_006718516.1:p.Glu483Gly
|
|
XM_006718454.2:c.1448A>G
|
XP_006718517.1:p.Glu483Gly
|
|
XM_006718456.2:c.1448A>G
|
XP_006718519.1:p.Glu483Gly
|
|
XM_011544802.1:c.1208A>G
|
XP_011543104.1:p.Glu403Gly
|
|
XM_011544803.1:c.1448A>G
|
XP_011543105.1:p.Glu483Gly
|
|
XM_011544804.1:c.1448A>G
|
XP_011543106.1:p.Glu483Gly
|
|
XM_011544805.1:c.1448A>G
|
XP_011543107.1:p.Glu483Gly
|
|
XM_011544806.1:c.1448A>G
|
XP_011543108.1:p.Glu483Gly
|
|
XM_011544807.1:c.752A>G
|
XP_011543109.1:p.Glu251Gly
|
|
XM_011544808.1:c.617A>G
|
XP_011543110.1:p.Glu206Gly
|
|
XR_247191.1:n.1549A>G
|
|
|
XM_005273824.4:c.1445A>G
|
XP_005273881.1:p.Glu482Gly
|
|
XM_005273826.4:c.1193A>G
|
XP_005273883.1:p.Glu398Gly
|
|
XM_005273830.4:c.755A>G
|
XP_005273887.1:p.Glu252Gly
|
|
XM_005273831.4:c.755A>G
|
XP_005273888.1:p.Glu252Gly
|
|
XM_005273832.4:c.725A>G
|
XP_005273889.1:p.Glu242Gly
|
|
XM_011544802.3:c.1208A>G
|
XP_011543104.1:p.Glu403Gly
|
|
XM_011544807.3:c.752A>G
|
XP_011543109.1:p.Glu251Gly
|
|
XM_011544808.3:c.617A>G
|
XP_011543110.1:p.Glu206Gly
|
|
XM_017017328.2:c.1279A>G
|
XP_016872817.1:p.Arg427Gly
|
|
XM_017017329.2:c.1276A>G
|
XP_016872818.1:p.Arg426Gly
|
|
XM_017017330.2:c.725A>G
|
XP_016872819.1:p.Glu242Gly
|
|
XM_017017331.2:c.725A>G
|
XP_016872820.1:p.Glu242Gly
|
|
XM_017017332.2:c.539A>G
|
XP_016872821.1:p.Glu180Gly
|
|
XM_017017333.2:c.556A>G
|
XP_016872822.1:p.Arg186Gly
|
|
XM_017017334.2:c.556A>G
|
XP_016872823.1:p.Arg186Gly
|
|
XM_017017335.2:c.556A>G
|
XP_016872824.1:p.Arg186Gly
|
|
XM_017017336.2:c.448A>G
|
XP_016872825.1:p.Arg150Gly
|
|
XM_024448392.1:c.1238A>G
|
XP_024304160.1:p.Glu413Gly
|
|
XM_024448393.1:c.725A>G
|
XP_024304161.1:p.Glu242Gly
|
|
XR_001747789.2:n.1380A>G
|
|
|
XR_001747790.2:n.1380A>G
|
|
|
XR_247191.3:n.1552A>G
|
|
|
NM_139075.4:c.1448A>G
MANE Select
|
NP_620714.2:p.Glu483Gly
|
|