ENST00000389266.8:c.884A>C
MANE Select
|
ENSP00000373918.3:p.Tyr295Ser
|
|
ENST00000444666.6:c.884A>C
|
ENSP00000415447.2:p.Tyr295Ser
|
|
ENST00000470392.2:n.974A>C
|
|
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ENST00000478124.6:n.947A>C
|
|
|
ENST00000485784.2:n.963A>C
|
|
|
ENST00000674616.1:c.*598A>C
|
ENSP00000502408.1:n.*598A>C
|
|
ENST00000674643.1:c.884A>C
|
ENSP00000501636.1:p.Tyr295Ser
|
|
ENST00000674734.1:n.1380A>C
|
|
|
ENST00000674737.1:c.*222A>C
|
ENSP00000502464.1:n.*222A>C
|
|
ENST00000674807.1:c.884A>C
|
ENSP00000502814.1:p.Tyr295Ser
|
|
ENST00000674815.1:c.515A>C
|
ENSP00000502799.1:p.Tyr172Ser
|
|
ENST00000674851.1:c.515A>C
|
ENSP00000502451.1:p.Tyr172Ser
|
|
ENST00000674969.1:n.2757A>C
|
|
|
ENST00000675051.1:c.683A>C
|
ENSP00000502296.1:p.Tyr228Ser
|
|
ENST00000675529.1:c.*754A>C
|
ENSP00000501655.1:n.*754A>C
|
|
ENST00000675587.1:n.900A>C
|
|
|
ENST00000675651.1:c.884A>C
|
ENSP00000502513.1:p.Tyr295Ser
|
|
ENST00000675693.1:c.716A>C
|
ENSP00000502174.1:p.Tyr239Ser
|
|
ENST00000675810.1:c.782A>C
|
ENSP00000502743.1:p.Tyr261Ser
|
|
ENST00000675859.1:c.884A>C
|
ENSP00000502033.1:p.Tyr295Ser
|
|
ENST00000675863.1:n.892A>C
|
|
|
ENST00000675886.1:n.6924A>C
|
|
|
ENST00000676088.1:c.*826A>C
|
ENSP00000501884.1:n.*826A>C
|
|
ENST00000676140.1:c.884A>C
|
ENSP00000502571.1:p.Tyr295Ser
|
|
ENST00000676164.1:c.*335A>C
|
ENSP00000501986.1:n.*335A>C
|
|
ENST00000676210.1:c.*173A>C
|
ENSP00000502373.1:n.*173A>C
|
|
ENST00000676259.1:c.*316A>C
|
ENSP00000501980.1:n.*316A>C
|
|
ENST00000676403.1:c.884A>C
|
ENSP00000502681.1:p.Tyr295Ser
|
|
ENST00000389266.7:c.884A>C
|
ENSP00000373918.3:p.Tyr295Ser
|
|
ENST00000478124.5:n.922A>C
|
|
|
NM_001316772.1:c.722A>C
|
NP_001303701.1:p.Tyr241Ser
|
|
NM_002047.2:c.884A>C , LRG_243t1:c.884A>C
|
NP_002038.2:p.Tyr295Ser
|
|
NM_002047.3:c.884A>C
|
NP_002038.2:p.Tyr295Ser
|
|
XM_006715686.1:c.515A>C
|
XP_006715749.1:p.Tyr172Ser
|
|
XM_006715686.2:c.515A>C
|
XP_006715749.1:p.Tyr172Ser
|
|
NM_002047.4:c.884A>C
MANE Select
|
NP_002038.2:p.Tyr295Ser
|
|