ENST00000692585.1:c.1058G=
|
ENSP00000509200.1:p.Gly353=
|
|
ENST00000294309.8:c.2201G=
MANE Select
|
ENSP00000294309.3:p.Gly734=
|
|
ENST00000635811.1:c.*396G=
|
ENSP00000490341.1:n.*396G=
|
|
ENST00000637084.1:c.1058G=
|
ENSP00000490615.1:p.Gly353=
|
|
ENST00000637342.1:c.2003+1965G=
|
ENSP00000490171.1:n.2003+1965G=
|
|
ENST00000637504.1:c.*33+2609G=
|
ENSP00000489759.1:n.*33+2609G=
|
|
ENST00000294309.7:c.2201G=
|
ENSP00000294309.3:p.Gly734=
|
|
ENST00000442692.2:n.1667G=
|
|
|
ENST00000542467.1:c.1655G=
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ENSP00000445551.1:p.Gly552=
|
|
NM_139075.3:c.2201G=
|
NP_620714.2:p.Gly734=
|
|
XM_005273824.2:c.2198G=
|
XP_005273881.1:p.Gly733=
|
|
XM_005273826.2:c.1946G=
|
XP_005273883.1:p.Gly649=
|
|
XM_005273830.2:c.1508G=
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XP_005273887.1:p.Gly503=
|
|
XM_005273831.2:c.1508G=
|
XP_005273888.1:p.Gly503=
|
|
XM_005273832.2:c.1478G=
|
XP_005273889.1:p.Gly493=
|
|
XM_006718453.2:c.1639+6396G=
|
XP_006718516.1:n.1639+6396G=
|
|
XM_006718454.2:c.1689+6396G=
|
XP_006718517.1:n.1689+6396G=
|
|
XM_011544802.1:c.1961G=
|
XP_011543104.1:p.Gly654=
|
|
XM_011544807.1:c.1505G=
|
XP_011543109.1:p.Gly502=
|
|
XM_011544808.1:c.1370G=
|
XP_011543110.1:p.Gly457=
|
|
XR_247191.1:n.2252G=
|
|
|
XM_005273824.4:c.2198G=
|
XP_005273881.1:p.Gly733=
|
|
XM_005273826.4:c.1946G=
|
XP_005273883.1:p.Gly649=
|
|
XM_005273830.4:c.1508G=
|
XP_005273887.1:p.Gly503=
|
|
XM_005273831.4:c.1508G=
|
XP_005273888.1:p.Gly503=
|
|
XM_005273832.4:c.1478G=
|
XP_005273889.1:p.Gly493=
|
|
XM_011544802.3:c.1961G=
|
XP_011543104.1:p.Gly654=
|
|
XM_011544807.3:c.1505G=
|
XP_011543109.1:p.Gly502=
|
|
XM_011544808.3:c.1370G=
|
XP_011543110.1:p.Gly457=
|
|
XM_017017328.2:c.1982G=
|
XP_016872817.1:p.Gly661=
|
|
XM_017017329.2:c.1979G=
|
XP_016872818.1:p.Gly660=
|
|
XM_017017330.2:c.1478G=
|
XP_016872819.1:p.Gly493=
|
|
XM_017017331.2:c.1478G=
|
XP_016872820.1:p.Gly493=
|
|
XM_017017332.2:c.1292G=
|
XP_016872821.1:p.Gly431=
|
|
XM_017017333.2:c.1259G=
|
XP_016872822.1:p.Gly420=
|
|
XM_017017334.2:c.1259G=
|
XP_016872823.1:p.Gly420=
|
|
XM_017017335.2:c.1259G=
|
XP_016872824.1:p.Gly420=
|
|
XM_017017336.2:c.1151G=
|
XP_016872825.1:p.Gly384=
|
|
XM_024448392.1:c.1991G=
|
XP_024304160.1:p.Gly664=
|
|
XM_024448393.1:c.1478G=
|
XP_024304161.1:p.Gly493=
|
|
XR_001747789.2:n.2133G=
|
|
|
XR_247191.3:n.2255G=
|
|
|
NM_139075.4:c.2201G=
MANE Select
|
NP_620714.2:p.Gly734=
|
|