ENST00000389054.8:c.1703C>A
MANE Select
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ENSP00000373706.4:p.Ala568Glu
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ENST00000647330.1:c.1680C>A
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ENSP00000494308.1:n.1680C>A
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ENST00000647433.1:c.1703C>A
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ENSP00000494675.1:p.Ala568Glu
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ENST00000253811.10:c.1571C>A
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ENSP00000253811.7:p.Ala524Glu
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ENST00000389054.7:c.1703C>A
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ENSP00000373706.4:p.Ala568Glu
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ENST00000389057.9:c.1676C>A
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ENSP00000373709.6:p.Ala559Glu
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ENST00000398557.8:c.1703C>A
|
ENSP00000381565.5:p.Ala568Glu
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ENST00000518047.5:c.1676C>A
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ENSP00000428268.2:p.Ala559Glu
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NM_001079812.2:c.1676C>A
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NP_001073280.1:p.Ala559Glu
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NM_001314007.1:c.1703C>A
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NP_001300936.1:p.Ala568Glu
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NM_005219.4:c.1703C>A
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NP_005210.3:p.Ala568Glu
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XM_011537572.1:c.1667C>A
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XP_011535874.1:p.Ala556Glu
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XM_011537573.1:c.1637C>A
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XP_011535875.1:p.Ala546Glu
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XM_024454384.1:c.1703C>A
|
XP_024310152.1:p.Ala568Glu
|
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XM_024454385.1:c.1676C>A
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XP_024310153.1:p.Ala559Glu
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XM_024454386.1:c.1667C>A
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XP_024310154.1:p.Ala556Glu
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XM_024454387.1:c.1637C>A
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XP_024310155.1:p.Ala546Glu
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NM_005219.5:c.1703C>A
MANE Select
|
NP_005210.3:p.Ala568Glu
|
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NM_001079812.3:c.1676C>A
|
NP_001073280.1:p.Ala559Glu
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|
NM_001314007.2:c.1703C>A
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NP_001300936.1:p.Ala568Glu
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