ENST00000255078.8:c.2562G>T
MANE Select
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ENSP00000255078.4:p.Gln854His
|
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ENST00000674675.1:c.707G>T
|
|
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ENST00000674878.1:c.667G>T
|
|
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ENST00000675118.1:c.2050G>T
|
|
|
ENST00000675389.1:n.837G>T
|
|
|
ENST00000675615.1:c.2562G>T
|
ENSP00000502413.1:p.Gln854His
|
|
ENST00000675648.1:n.1937G>T
|
|
|
ENST00000675916.1:c.806G>T
|
|
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ENST00000676173.1:n.3307G>T
|
|
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ENST00000676182.1:c.993G>T
|
|
|
ENST00000676228.1:c.*1885G>T
|
ENSP00000502375.1:n.*1885G>T
|
|
ENST00000255078.7:c.2562G>T
|
ENSP00000255078.3:p.Gln854His
|
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ENST00000539064.5:n.2321G>T
|
|
|
ENST00000543739.5:n.1555G>T
|
|
|
NM_002180.2:c.2562G>T , LRG_250t1:c.2562G>T
|
NP_002171.2:p.Gln854His
|
|
XM_005273974.2:c.1551G>T
|
XP_005274031.1:p.Gln517His
|
|
XM_005273975.2:c.1434G>T
|
XP_005274032.1:p.Gln478His
|
|
XM_011544994.1:c.1329G>T
|
XP_011543296.1:p.Gln443His
|
|
XR_949903.1:n.2664G>T
|
|
|
XM_005273975.3:c.1434G>T
|
XP_005274032.1:p.Gln478His
|
|
XM_017017669.2:c.1551G>T
|
XP_016873158.1:p.Gln517His
|
|
XM_017017670.2:c.1551G>T
|
XP_016873159.1:p.Gln517His
|
|
XR_949903.3:n.2660G>T
|
|
|
NM_002180.3:c.2562G>T
MANE Select
|
NP_002171.2:p.Gln854His
|
|