ENST00000255078.8:c.1799C>T
MANE Select
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ENSP00000255078.4:p.Ala600Val
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ENST00000674675.1:c.43C>T
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ENST00000674878.1:c.43C>T
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ENST00000674955.1:c.*516C>T
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ENSP00000502463.1:n.*516C>T
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ENST00000675118.1:c.1287C>T
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|
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ENST00000675389.1:n.74C>T
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ENST00000675615.1:c.1799C>T
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ENSP00000502413.1:p.Ala600Val
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ENST00000675648.1:n.1174C>T
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|
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ENST00000675916.1:c.43C>T
|
|
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ENST00000676173.1:n.2544C>T
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ENST00000676182.1:c.230C>T
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|
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ENST00000676228.1:c.*1122C>T
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ENSP00000502375.1:n.*1122C>T
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ENST00000255078.7:c.1799C>T
|
ENSP00000255078.3:p.Ala600Val
|
|
ENST00000539064.5:n.1558C>T
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|
|
ENST00000541229.5:n.494C>T
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|
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ENST00000543739.5:n.792C>T
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ENST00000545475.1:n.395C>T
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NM_002180.2:c.1799C>T , LRG_250t1:c.1799C>T
|
NP_002171.2:p.Ala600Val
|
|
XM_005273974.2:c.788C>T
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XP_005274031.1:p.Ala263Val
|
|
XM_005273975.2:c.671C>T
|
XP_005274032.1:p.Ala224Val
|
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XM_011544994.1:c.566C>T
|
XP_011543296.1:p.Ala189Val
|
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XR_949903.1:n.1901C>T
|
|
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XM_005273975.3:c.671C>T
|
XP_005274032.1:p.Ala224Val
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XM_017017669.2:c.788C>T
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XP_016873158.1:p.Ala263Val
|
|
XM_017017670.2:c.788C>T
|
XP_016873159.1:p.Ala263Val
|
|
XR_949903.3:n.1897C>T
|
|
|
NM_002180.3:c.1799C>T
MANE Select
|
NP_002171.2:p.Ala600Val
|
|