ENST00000255078.8:c.2010T>C
MANE Select
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ENSP00000255078.4:p.Ala670=
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ENST00000674675.1:c.254T>C
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|
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ENST00000674878.1:c.254T>C
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|
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ENST00000674955.1:c.*727T>C
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ENSP00000502463.1:n.*727T>C
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ENST00000675118.1:c.1498T>C
|
|
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ENST00000675389.1:n.285T>C
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|
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ENST00000675615.1:c.2010T>C
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ENSP00000502413.1:p.Ala670=
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ENST00000675648.1:n.1385T>C
|
|
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ENST00000675916.1:c.254T>C
|
|
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ENST00000676173.1:n.2755T>C
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ENST00000676182.1:c.441T>C
|
|
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ENST00000676228.1:c.*1333T>C
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ENSP00000502375.1:n.*1333T>C
|
|
ENST00000255078.7:c.2010T>C
|
ENSP00000255078.3:p.Ala670=
|
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ENST00000539064.5:n.1769T>C
|
|
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ENST00000543739.5:n.1003T>C
|
|
|
NM_002180.2:c.2010T>C , LRG_250t1:c.2010T>C
|
NP_002171.2:p.Ala670=
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XM_005273974.2:c.999T>C
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XP_005274031.1:p.Ala333=
|
|
XM_005273975.2:c.882T>C
|
XP_005274032.1:p.Ala294=
|
|
XM_011544994.1:c.777T>C
|
XP_011543296.1:p.Ala259=
|
|
XR_949903.1:n.2112T>C
|
|
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XM_005273975.3:c.882T>C
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XP_005274032.1:p.Ala294=
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XM_017017669.2:c.999T>C
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XP_016873158.1:p.Ala333=
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|
XM_017017670.2:c.999T>C
|
XP_016873159.1:p.Ala333=
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XR_949903.3:n.2108T>C
|
|
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NM_002180.3:c.2010T>C
MANE Select
|
NP_002171.2:p.Ala670=
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