ENST00000380707.9:c.819T>A
MANE Select
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ENSP00000370083.4:p.His273Gln
|
|
ENST00000351205.8:c.819T>A
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ENSP00000305857.5:p.His273Gln
|
|
ENST00000380707.8:c.819T>A
|
ENSP00000370083.4:p.His273Gln
|
|
ENST00000503079.6:c.723T>A
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ENSP00000428128.1:p.His241Gln
|
|
ENST00000506163.5:c.819T>A
|
ENSP00000424926.1:p.His273Gln
|
|
ENST00000506239.6:c.819T>A
|
ENSP00000422679.2:p.His273Gln
|
|
ENST00000510679.1:n.73T>A
|
|
|
ENST00000513228.1:n.386T>A
|
|
|
ENST00000514951.5:c.618T>A
|
ENSP00000423298.1:p.His206Gln
|
|
ENST00000518504.5:n.336T>A
|
|
|
ENST00000625245.2:c.819T>A
|
ENSP00000486539.1:p.His273Gln
|
|
NM_000344.3:c.819T>A , LRG_676t1:c.819T>A
|
NP_000335.1:p.His273Gln
|
|
NM_001297715.1:c.819T>A
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NP_001284644.1:p.His273Gln
|
|
NM_022874.2:c.723T>A
|
NP_075012.1:p.His241Gln
|
|
XM_011543596.1:c.819T>A
|
XP_011541898.1:p.His273Gln
|
|
XM_011543597.1:c.618T>A
|
XP_011541899.1:p.His206Gln
|
|
XM_011543598.1:c.522T>A
|
XP_011541900.1:p.His174Gln
|
|
XM_011543598.3:c.522T>A
|
XP_011541900.1:p.His174Gln
|
|
XM_017009786.1:c.723T>A
|
XP_016865275.1:p.His241Gln
|
|
NM_000344.4:c.819T>A
MANE Select
|
NP_000335.1:p.His273Gln
|
|