ENST00000350026.11:c.4610C>A
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ENSP00000055163.8:p.Ala1537Glu
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ENST00000414678.8:c.4679C>A
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ENSP00000412835.3:p.Ala1560Glu
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ENST00000637015.2:c.4898C>A
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ENSP00000489729.2:p.Ala1633Glu
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ENST00000346085.10:c.4649C>A
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ENSP00000344546.5:p.Ala1550Glu
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ENST00000350026.10:c.4361C>A
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ENSP00000055163.7:p.Ala1454Glu
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ENST00000414678.7:c.2927C>A
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ENSP00000412835.2:p.Ala976Glu
|
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ENST00000635849.1:c.2090C>A
|
ENSP00000490948.1:p.Ala697Glu
|
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ENST00000635957.1:c.1721C>A
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ENSP00000490385.1:p.Ala574Glu
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ENST00000636227.1:n.3232C>A
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ENST00000636254.1:n.689C>A
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|
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ENST00000636930.2:c.4769C>A
MANE Select
|
ENSP00000490491.2:p.Ala1590Glu
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ENST00000636940.1:n.2766C>A
|
|
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ENST00000637015.1:c.2137C>A
|
|
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ENST00000637568.1:c.2051C>A
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|
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ENST00000637741.1:n.1435C>A
|
|
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ENST00000637810.1:c.2111C>A
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ENSP00000489636.1:p.Ala704Glu
|
|
ENST00000637904.1:c.2270C>A
|
ENSP00000490550.1:p.Ala757Glu
|
|
ENST00000647938.1:c.4400C>A
|
ENSP00000498155.1:p.Ala1467Glu
|
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ENST00000346085.9:c.4400C>A
|
ENSP00000344546.4:p.Ala1467Glu
|
|
ENST00000350026.9:c.4361C>A
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ENSP00000055163.7:p.Ala1454Glu
|
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ENST00000414678.6:c.2927C>A
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ENSP00000412835.2:p.Ala976Glu
|
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NM_017519.2:c.4361C>A
|
NP_059989.2:p.Ala1454Glu
|
|
NM_020732.3:c.4400C>A
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NP_065783.3:p.Ala1467Glu
|
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XM_005267069.3:c.4520C>A
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XP_005267126.2:p.Ala1507Glu
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XM_011535984.1:c.3599C>A
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XP_011534286.1:p.Ala1200Glu
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XM_011535985.1:c.3419C>A
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XP_011534287.1:p.Ala1140Glu
|
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XM_011535986.1:c.3179C>A
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XP_011534288.1:p.Ala1060Glu
|
|
XM_011535987.1:c.2798C>A
|
XP_011534289.1:p.Ala933Glu
|
|
XM_011535988.1:c.1661C>A
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XP_011534290.1:p.Ala554Glu
|
|
NM_001346813.1:c.4520C>A
|
NP_001333742.1:p.Ala1507Glu
|
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NM_001363725.1:c.2270C>A
|
NP_001350654.1:p.Ala757Glu
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|
XM_011535984.2:c.4730C>A
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XP_011534286.2:p.Ala1577Glu
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XM_011535988.3:c.1661C>A
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XP_011534290.1:p.Ala554Glu
|
|
XM_017011103.2:c.4631C>A
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XP_016866592.1:p.Ala1544Glu
|
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XM_017011104.1:c.4601C>A
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XP_016866593.1:p.Ala1534Glu
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XM_017011105.2:c.4571C>A
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XP_016866594.1:p.Ala1524Glu
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XM_017011106.2:c.4442C>A
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XP_016866595.1:p.Ala1481Glu
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XM_017011107.2:c.4421C>A
|
XP_016866596.1:p.Ala1474Glu
|
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XR_002956289.1:n.4716C>A
|
|
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NM_001363725.2:c.2270C>A
|
NP_001350654.1:p.Ala757Glu
|
|
NM_001371656.1:c.4649C>A
|
NP_001358585.1:p.Ala1550Glu
|
|
NM_001374820.1:c.4649C>A
|
NP_001361749.1:p.Ala1550Glu
|
|
NM_001374828.1:c.4769C>A
MANE Select
|
NP_001361757.1:p.Ala1590Glu
|
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NM_017519.3:c.4610C>A
|
NP_059989.3:p.Ala1537Glu
|
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