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ENST00000675419.1:c.484_485delinsGC
MANE Select
|
ENSP00000501943.1:p.Arg162Ala
|
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ENST00000300305.7:c.484_485delinsGC
|
ENSP00000300305.3:p.Arg162Ala
|
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ENST00000344691.8:c.403_404delinsGC
|
ENSP00000340690.4:p.Arg135Ala
|
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ENST00000358356.9:c.403_404delinsGC
|
ENSP00000351123.5:p.Arg135Ala
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ENST00000399237.6:c.448_449delinsGC
|
ENSP00000382182.2:p.Arg150Ala
|
|
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ENST00000399240.5:c.403_404delinsGC
|
ENSP00000382184.1:p.Arg135Ala
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ENST00000437180.5:c.484_485delinsGC
|
ENSP00000409227.1:p.Arg162Ala
|
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ENST00000482318.5:c.*74_*75delinsGC
|
ENSP00000477067.1:n.*74_*75delinsGC
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NM_001001890.2:c.403_404delinsGC
|
NP_001001890.1:p.Arg135Ala
|
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NM_001122607.1:c.403_404delinsGC
|
NP_001116079.1:p.Arg135Ala
|
|
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NM_001754.4:c.484_485delinsGC , LRG_482t1:c.484_485delinsGC
|
NP_001745.2:p.Arg162Ala
|
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XM_005261068.3:c.448_449delinsGC
|
XP_005261125.1:p.Arg150Ala
|
|
|
XM_005261069.3:c.484_485delinsGC
|
XP_005261126.1:p.Arg162Ala
|
|
|
XM_011529766.1:c.484_485delinsGC
|
XP_011528068.1:p.Arg162Ala
|
|
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XM_011529767.1:c.445_446delinsGC
|
XP_011528069.1:p.Arg149Ala
|
|
|
XM_011529768.1:c.445_446delinsGC
|
XP_011528070.1:p.Arg149Ala
|
|
|
XM_011529770.1:c.484_485delinsGC
|
XP_011528072.1:p.Arg162Ala
|
|
|
XR_937576.1:n.663_664delinsGC
|
|
|
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XM_005261069.4:c.484_485delinsGC
|
XP_005261126.1:p.Arg162Ala
|
|
|
XM_011529766.2:c.484_485delinsGC
|
XP_011528068.1:p.Arg162Ala
|
|
|
XM_011529767.2:c.445_446delinsGC
|
XP_011528069.1:p.Arg149Ala
|
|
|
XM_011529768.2:c.445_446delinsGC
|
XP_011528070.1:p.Arg149Ala
|
|
|
XM_011529770.2:c.484_485delinsGC
|
XP_011528072.1:p.Arg162Ala
|
|
|
XM_017028487.1:c.331_332delinsGC
|
XP_016883976.1:p.Arg111Ala
|
|
|
XR_937576.2:n.710_711delinsGC
|
|
|
|
NM_001001890.3:c.403_404delinsGC
|
NP_001001890.1:p.Arg135Ala
|
|
|
NM_001122607.2:c.403_404delinsGC
|
NP_001116079.1:p.Arg135Ala
|
|
|
NM_001754.5:c.484_485delinsGC
MANE Select
|
NP_001745.2:p.Arg162Ala
|
|
