ENST00000692585.1:c.1061A>C
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ENSP00000509200.1:p.Glu354Ala
|
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ENST00000294309.8:c.2204A>C
MANE Select
|
ENSP00000294309.3:p.Glu735Ala
|
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ENST00000635811.1:c.*399A>C
|
ENSP00000490341.1:n.*399A>C
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|
ENST00000637084.1:c.1061A>C
|
ENSP00000490615.1:p.Glu354Ala
|
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ENST00000637342.1:c.2003+1968A>C
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ENSP00000490171.1:n.2003+1968A>C
|
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ENST00000637504.1:c.*33+2612A>C
|
ENSP00000489759.1:n.*33+2612A>C
|
|
ENST00000294309.7:c.2204A>C
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ENSP00000294309.3:p.Glu735Ala
|
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ENST00000442692.2:n.1670A>C
|
|
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ENST00000542467.1:c.1658A>C
|
ENSP00000445551.1:p.Glu553Ala
|
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NM_139075.3:c.2204A>C
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NP_620714.2:p.Glu735Ala
|
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XM_005273824.2:c.2201A>C
|
XP_005273881.1:p.Glu734Ala
|
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XM_005273826.2:c.1949A>C
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XP_005273883.1:p.Glu650Ala
|
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XM_005273830.2:c.1511A>C
|
XP_005273887.1:p.Glu504Ala
|
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XM_005273831.2:c.1511A>C
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XP_005273888.1:p.Glu504Ala
|
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XM_005273832.2:c.1481A>C
|
XP_005273889.1:p.Glu494Ala
|
|
XM_006718453.2:c.1639+6399A>C
|
XP_006718516.1:n.1639+6399A>C
|
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XM_006718454.2:c.1689+6399A>C
|
XP_006718517.1:n.1689+6399A>C
|
|
XM_011544802.1:c.1964A>C
|
XP_011543104.1:p.Glu655Ala
|
|
XM_011544807.1:c.1508A>C
|
XP_011543109.1:p.Glu503Ala
|
|
XM_011544808.1:c.1373A>C
|
XP_011543110.1:p.Glu458Ala
|
|
XR_247191.1:n.2255A>C
|
|
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XM_005273824.4:c.2201A>C
|
XP_005273881.1:p.Glu734Ala
|
|
XM_005273826.4:c.1949A>C
|
XP_005273883.1:p.Glu650Ala
|
|
XM_005273830.4:c.1511A>C
|
XP_005273887.1:p.Glu504Ala
|
|
XM_005273831.4:c.1511A>C
|
XP_005273888.1:p.Glu504Ala
|
|
XM_005273832.4:c.1481A>C
|
XP_005273889.1:p.Glu494Ala
|
|
XM_011544802.3:c.1964A>C
|
XP_011543104.1:p.Glu655Ala
|
|
XM_011544807.3:c.1508A>C
|
XP_011543109.1:p.Glu503Ala
|
|
XM_011544808.3:c.1373A>C
|
XP_011543110.1:p.Glu458Ala
|
|
XM_017017328.2:c.1985A>C
|
XP_016872817.1:p.Glu662Ala
|
|
XM_017017329.2:c.1982A>C
|
XP_016872818.1:p.Glu661Ala
|
|
XM_017017330.2:c.1481A>C
|
XP_016872819.1:p.Glu494Ala
|
|
XM_017017331.2:c.1481A>C
|
XP_016872820.1:p.Glu494Ala
|
|
XM_017017332.2:c.1295A>C
|
XP_016872821.1:p.Glu432Ala
|
|
XM_017017333.2:c.1262A>C
|
XP_016872822.1:p.Glu421Ala
|
|
XM_017017334.2:c.1262A>C
|
XP_016872823.1:p.Glu421Ala
|
|
XM_017017335.2:c.1262A>C
|
XP_016872824.1:p.Glu421Ala
|
|
XM_017017336.2:c.1154A>C
|
XP_016872825.1:p.Glu385Ala
|
|
XM_024448392.1:c.1994A>C
|
XP_024304160.1:p.Glu665Ala
|
|
XM_024448393.1:c.1481A>C
|
XP_024304161.1:p.Glu494Ala
|
|
XR_001747789.2:n.2136A>C
|
|
|
XR_247191.3:n.2258A>C
|
|
|
NM_139075.4:c.2204A>C
MANE Select
|
NP_620714.2:p.Glu735Ala
|
|