ENST00000692585.1:c.1076A>T
|
ENSP00000509200.1:p.Glu359Val
|
|
ENST00000294309.8:c.2219A>T
MANE Select
|
ENSP00000294309.3:p.Glu740Val
|
|
ENST00000635811.1:c.*414A>T
|
ENSP00000490341.1:n.*414A>T
|
|
ENST00000637084.1:c.1076A>T
|
ENSP00000490615.1:p.Glu359Val
|
|
ENST00000637342.1:c.2003+1983A>T
|
ENSP00000490171.1:n.2003+1983A>T
|
|
ENST00000637504.1:c.*33+2627A>T
|
ENSP00000489759.1:n.*33+2627A>T
|
|
ENST00000294309.7:c.2219A>T
|
ENSP00000294309.3:p.Glu740Val
|
|
ENST00000442692.2:n.1685A>T
|
|
|
ENST00000542467.1:c.1673A>T
|
ENSP00000445551.1:p.Glu558Val
|
|
NM_139075.3:c.2219A>T
|
NP_620714.2:p.Glu740Val
|
|
XM_005273824.2:c.2216A>T
|
XP_005273881.1:p.Glu739Val
|
|
XM_005273826.2:c.1964A>T
|
XP_005273883.1:p.Glu655Val
|
|
XM_005273830.2:c.1526A>T
|
XP_005273887.1:p.Glu509Val
|
|
XM_005273831.2:c.1526A>T
|
XP_005273888.1:p.Glu509Val
|
|
XM_005273832.2:c.1496A>T
|
XP_005273889.1:p.Glu499Val
|
|
XM_006718453.2:c.1639+6414A>T
|
XP_006718516.1:n.1639+6414A>T
|
|
XM_006718454.2:c.1689+6414A>T
|
XP_006718517.1:n.1689+6414A>T
|
|
XM_011544802.1:c.1979A>T
|
XP_011543104.1:p.Glu660Val
|
|
XM_011544807.1:c.1523A>T
|
XP_011543109.1:p.Glu508Val
|
|
XM_011544808.1:c.1388A>T
|
XP_011543110.1:p.Glu463Val
|
|
XR_247191.1:n.2270A>T
|
|
|
XM_005273824.4:c.2216A>T
|
XP_005273881.1:p.Glu739Val
|
|
XM_005273826.4:c.1964A>T
|
XP_005273883.1:p.Glu655Val
|
|
XM_005273830.4:c.1526A>T
|
XP_005273887.1:p.Glu509Val
|
|
XM_005273831.4:c.1526A>T
|
XP_005273888.1:p.Glu509Val
|
|
XM_005273832.4:c.1496A>T
|
XP_005273889.1:p.Glu499Val
|
|
XM_011544802.3:c.1979A>T
|
XP_011543104.1:p.Glu660Val
|
|
XM_011544807.3:c.1523A>T
|
XP_011543109.1:p.Glu508Val
|
|
XM_011544808.3:c.1388A>T
|
XP_011543110.1:p.Glu463Val
|
|
XM_017017328.2:c.2000A>T
|
XP_016872817.1:p.Glu667Val
|
|
XM_017017329.2:c.1997A>T
|
XP_016872818.1:p.Glu666Val
|
|
XM_017017330.2:c.1496A>T
|
XP_016872819.1:p.Glu499Val
|
|
XM_017017331.2:c.1496A>T
|
XP_016872820.1:p.Glu499Val
|
|
XM_017017332.2:c.1310A>T
|
XP_016872821.1:p.Glu437Val
|
|
XM_017017333.2:c.1277A>T
|
XP_016872822.1:p.Glu426Val
|
|
XM_017017334.2:c.1277A>T
|
XP_016872823.1:p.Glu426Val
|
|
XM_017017335.2:c.1277A>T
|
XP_016872824.1:p.Glu426Val
|
|
XM_017017336.2:c.1169A>T
|
XP_016872825.1:p.Glu390Val
|
|
XM_024448392.1:c.2009A>T
|
XP_024304160.1:p.Glu670Val
|
|
XM_024448393.1:c.1496A>T
|
XP_024304161.1:p.Glu499Val
|
|
XR_001747789.2:n.2151A>T
|
|
|
XR_247191.3:n.2273A>T
|
|
|
NM_139075.4:c.2219A>T
MANE Select
|
NP_620714.2:p.Glu740Val
|
|