ENST00000255078.8:c.1905A>C
MANE Select
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ENSP00000255078.4:p.Glu635Asp
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ENST00000674675.1:c.149A>C
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|
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ENST00000674878.1:c.149A>C
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ENST00000674955.1:c.*622A>C
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ENSP00000502463.1:n.*622A>C
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ENST00000675118.1:c.1393A>C
|
|
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ENST00000675389.1:n.180A>C
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|
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ENST00000675615.1:c.1905A>C
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ENSP00000502413.1:p.Glu635Asp
|
|
ENST00000675648.1:n.1280A>C
|
|
|
ENST00000675916.1:c.149A>C
|
|
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ENST00000676173.1:n.2650A>C
|
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ENST00000676182.1:c.336A>C
|
|
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ENST00000676228.1:c.*1228A>C
|
ENSP00000502375.1:n.*1228A>C
|
|
ENST00000255078.7:c.1905A>C
|
ENSP00000255078.3:p.Glu635Asp
|
|
ENST00000539064.5:n.1664A>C
|
|
|
ENST00000543739.5:n.898A>C
|
|
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ENST00000545475.1:n.501A>C
|
|
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NM_002180.2:c.1905A>C , LRG_250t1:c.1905A>C
|
NP_002171.2:p.Glu635Asp
|
|
XM_005273974.2:c.894A>C
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XP_005274031.1:p.Glu298Asp
|
|
XM_005273975.2:c.777A>C
|
XP_005274032.1:p.Glu259Asp
|
|
XM_011544994.1:c.672A>C
|
XP_011543296.1:p.Glu224Asp
|
|
XR_949903.1:n.2007A>C
|
|
|
XM_005273975.3:c.777A>C
|
XP_005274032.1:p.Glu259Asp
|
|
XM_017017669.2:c.894A>C
|
XP_016873158.1:p.Glu298Asp
|
|
XM_017017670.2:c.894A>C
|
XP_016873159.1:p.Glu298Asp
|
|
XR_949903.3:n.2003A>C
|
|
|
NM_002180.3:c.1905A>C
MANE Select
|
NP_002171.2:p.Glu635Asp
|
|