ENST00000350026.11:c.4607C>A
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ENSP00000055163.8:p.Ala1536Glu
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ENST00000414678.8:c.4676C>A
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ENSP00000412835.3:p.Ala1559Glu
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ENST00000637015.2:c.4895C>A
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ENSP00000489729.2:p.Ala1632Glu
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ENST00000346085.10:c.4646C>A
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ENSP00000344546.5:p.Ala1549Glu
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ENST00000350026.10:c.4358C>A
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ENSP00000055163.7:p.Ala1453Glu
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ENST00000414678.7:c.2924C>A
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ENSP00000412835.2:p.Ala975Glu
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ENST00000635849.1:c.2087C>A
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ENSP00000490948.1:p.Ala696Glu
|
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ENST00000635957.1:c.1718C>A
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ENSP00000490385.1:p.Ala573Glu
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ENST00000636227.1:n.3229C>A
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ENST00000636254.1:n.686C>A
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|
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ENST00000636930.2:c.4766C>A
MANE Select
|
ENSP00000490491.2:p.Ala1589Glu
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ENST00000636940.1:n.2763C>A
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|
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ENST00000637015.1:c.2134C>A
|
|
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ENST00000637568.1:c.2048C>A
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|
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ENST00000637741.1:n.1432C>A
|
|
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ENST00000637810.1:c.2108C>A
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ENSP00000489636.1:p.Ala703Glu
|
|
ENST00000637904.1:c.2267C>A
|
ENSP00000490550.1:p.Ala756Glu
|
|
ENST00000647938.1:c.4397C>A
|
ENSP00000498155.1:p.Ala1466Glu
|
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ENST00000346085.9:c.4397C>A
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ENSP00000344546.4:p.Ala1466Glu
|
|
ENST00000350026.9:c.4358C>A
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ENSP00000055163.7:p.Ala1453Glu
|
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ENST00000414678.6:c.2924C>A
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ENSP00000412835.2:p.Ala975Glu
|
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NM_017519.2:c.4358C>A
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NP_059989.2:p.Ala1453Glu
|
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NM_020732.3:c.4397C>A
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NP_065783.3:p.Ala1466Glu
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XM_005267069.3:c.4517C>A
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XP_005267126.2:p.Ala1506Glu
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XM_011535984.1:c.3596C>A
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XP_011534286.1:p.Ala1199Glu
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XM_011535985.1:c.3416C>A
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XP_011534287.1:p.Ala1139Glu
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XM_011535986.1:c.3176C>A
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XP_011534288.1:p.Ala1059Glu
|
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XM_011535987.1:c.2795C>A
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XP_011534289.1:p.Ala932Glu
|
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XM_011535988.1:c.1658C>A
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XP_011534290.1:p.Ala553Glu
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NM_001346813.1:c.4517C>A
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NP_001333742.1:p.Ala1506Glu
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NM_001363725.1:c.2267C>A
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NP_001350654.1:p.Ala756Glu
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XM_011535984.2:c.4727C>A
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XP_011534286.2:p.Ala1576Glu
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XM_011535988.3:c.1658C>A
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XP_011534290.1:p.Ala553Glu
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XM_017011103.2:c.4628C>A
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XP_016866592.1:p.Ala1543Glu
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XM_017011104.1:c.4598C>A
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XP_016866593.1:p.Ala1533Glu
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XM_017011105.2:c.4568C>A
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XP_016866594.1:p.Ala1523Glu
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XM_017011106.2:c.4439C>A
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XP_016866595.1:p.Ala1480Glu
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XM_017011107.2:c.4418C>A
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XP_016866596.1:p.Ala1473Glu
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XR_002956289.1:n.4713C>A
|
|
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NM_001363725.2:c.2267C>A
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NP_001350654.1:p.Ala756Glu
|
|
NM_001371656.1:c.4646C>A
|
NP_001358585.1:p.Ala1549Glu
|
|
NM_001374820.1:c.4646C>A
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NP_001361749.1:p.Ala1549Glu
|
|
NM_001374828.1:c.4766C>A
MANE Select
|
NP_001361757.1:p.Ala1589Glu
|
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NM_017519.3:c.4607C>A
|
NP_059989.3:p.Ala1536Glu
|
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