ENST00000460843.6:c.1818G>C
MANE Select
|
ENSP00000417980.1:p.Glu606Asp
|
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ENST00000636027.1:c.1704G>C
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ENSP00000489961.1:p.Glu568Asp
|
|
ENST00000637161.1:c.1725G>C
|
ENSP00000490328.1:p.Glu575Asp
|
|
ENST00000637261.1:c.1858G>C
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ENSP00000490815.1:n.1858G>C
|
|
ENST00000638071.1:c.1445G>C
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|
|
ENST00000640639.1:c.987G>C
|
ENSP00000491823.1:p.Glu329Asp
|
|
ENST00000371394.6:c.*1553G>C
|
ENSP00000485945.1:n.*1553G>C
|
|
ENST00000460843.5:c.1818G>C
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ENSP00000417980.1:p.Glu606Asp
|
|
ENST00000462484.5:c.1818G>C
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ENSP00000417328.1:p.Glu606Asp
|
|
ENST00000462942.3:c.675G>C
|
ENSP00000436107.1:p.Glu225Asp
|
|
ENST00000465566.2:c.366G>C
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ENSP00000486261.1:p.Glu122Asp
|
|
ENST00000626603.1:n.1805C>G
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|
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NM_001145527.1:c.1818G>C
|
NP_001138999.1:p.Glu606Asp
|
|
NM_024757.4:c.1818G>C
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NP_079033.4:p.Glu606Asp
|
|
XM_005266105.3:c.1809G>C
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XP_005266162.1:p.Glu603Asp
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|
XM_005266110.1:c.1725G>C
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XP_005266167.1:p.Glu575Asp
|
|
XM_006717288.2:c.1800G>C
|
XP_006717351.1:p.Glu600Asp
|
|
XM_011519021.1:c.1827G>C
|
XP_011517323.1:p.Glu609Asp
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|
XM_011519022.1:c.1824G>C
|
XP_011517324.1:p.Glu608Asp
|
|
XM_011519023.1:c.1806G>C
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XP_011517325.1:p.Glu602Asp
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|
XM_011519024.1:c.1749G>C
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XP_011517326.1:p.Glu583Asp
|
|
XM_011519025.1:c.1725G>C
|
XP_011517327.1:p.Glu575Asp
|
|
XM_011519026.1:c.1683G>C
|
XP_011517328.1:p.Glu561Asp
|
|
XM_011519027.1:c.1827G>C
|
XP_011517329.1:p.Glu609Asp
|
|
XM_011519028.1:c.1827G>C
|
XP_011517330.1:p.Glu609Asp
|
|
XM_011519029.1:c.249G>C
|
XP_011517331.1:p.Glu83Asp
|
|
XM_011519033.1:c.1662G>C
|
XP_011517335.1:p.Glu554Asp
|
|
NM_001354259.1:c.1725G>C
|
NP_001341188.1:p.Glu575Asp
|
|
NM_001354263.1:c.1797G>C
|
NP_001341192.1:p.Glu599Asp
|
|
XM_005266105.5:c.1809G>C
|
XP_005266162.1:p.Glu603Asp
|
|
XM_011519021.3:c.1827G>C
|
XP_011517323.1:p.Glu609Asp
|
|
XM_011519022.3:c.1824G>C
|
XP_011517324.1:p.Glu608Asp
|
|
XM_011519023.3:c.1806G>C
|
XP_011517325.1:p.Glu602Asp
|
|
XM_011519029.3:c.249G>C
|
XP_011517331.1:p.Glu83Asp
|
|
XM_017015134.1:c.1803G>C
|
XP_016870623.1:p.Glu601Asp
|
|
XM_017015136.2:c.1719G>C
|
XP_016870625.1:p.Glu573Asp
|
|
XM_017015137.1:c.1704G>C
|
XP_016870626.1:p.Glu568Asp
|
|
XM_017015138.1:c.1704G>C
|
XP_016870627.1:p.Glu568Asp
|
|
XM_024447674.1:c.1647G>C
|
XP_024303442.1:p.Glu549Asp
|
|
XM_024447675.1:c.1581G>C
|
XP_024303443.1:p.Glu527Asp
|
|
XM_024447676.1:c.942G>C
|
XP_024303444.1:p.Glu314Asp
|
|
XM_024447677.1:c.942G>C
|
XP_024303445.1:p.Glu314Asp
|
|
XM_024447678.1:c.1725G>C
|
XP_024303446.1:p.Glu575Asp
|
|
XM_024447679.1:c.1725G>C
|
XP_024303447.1:p.Glu575Asp
|
|
XM_024447680.1:c.1560G>C
|
XP_024303448.1:p.Glu520Asp
|
|
NM_024757.5:c.1818G>C
MANE Select
|
NP_079033.4:p.Glu606Asp
|
|
NM_001145527.2:c.1818G>C
|
NP_001138999.1:p.Glu606Asp
|
|
NM_001354259.2:c.1725G>C
|
NP_001341188.1:p.Glu575Asp
|
|
NM_001354263.2:c.1797G>C
|
NP_001341192.1:p.Glu599Asp
|
|