ENST00000255078.8:c.2153A>T
MANE Select
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ENSP00000255078.4:p.Glu718Val
|
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ENST00000674675.1:c.397A>T
|
|
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ENST00000674878.1:c.397A>T
|
|
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ENST00000674955.1:c.*870A>T
|
ENSP00000502463.1:n.*870A>T
|
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ENST00000675118.1:c.1641A>T
|
|
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ENST00000675389.1:n.428A>T
|
|
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ENST00000675615.1:c.2153A>T
|
ENSP00000502413.1:p.Glu718Val
|
|
ENST00000675648.1:n.1528A>T
|
|
|
ENST00000675916.1:c.397A>T
|
|
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ENST00000676173.1:n.2898A>T
|
|
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ENST00000676182.1:c.584A>T
|
|
|
ENST00000676228.1:c.*1476A>T
|
ENSP00000502375.1:n.*1476A>T
|
|
ENST00000255078.7:c.2153A>T
|
ENSP00000255078.3:p.Glu718Val
|
|
ENST00000539064.5:n.1912A>T
|
|
|
ENST00000543739.5:n.1146A>T
|
|
|
NM_002180.2:c.2153A>T , LRG_250t1:c.2153A>T
|
NP_002171.2:p.Glu718Val
|
|
XM_005273974.2:c.1142A>T
|
XP_005274031.1:p.Glu381Val
|
|
XM_005273975.2:c.1025A>T
|
XP_005274032.1:p.Glu342Val
|
|
XM_011544994.1:c.920A>T
|
XP_011543296.1:p.Glu307Val
|
|
XR_949903.1:n.2255A>T
|
|
|
XM_005273975.3:c.1025A>T
|
XP_005274032.1:p.Glu342Val
|
|
XM_017017669.2:c.1142A>T
|
XP_016873158.1:p.Glu381Val
|
|
XM_017017670.2:c.1142A>T
|
XP_016873159.1:p.Glu381Val
|
|
XR_949903.3:n.2251A>T
|
|
|
NM_002180.3:c.2153A>T
MANE Select
|
NP_002171.2:p.Glu718Val
|
|