ENST00000382276.8:c.734G>T
MANE Select
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ENSP00000371711.3:p.Gly245Val
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ENST00000382276.7:c.734G>T
|
ENSP00000371711.3:p.Gly245Val
|
|
ENST00000564322.1:n.883G>T
|
|
|
ENST00000569227.1:c.260G>T
|
ENSP00000454701.1:p.Gly87Val
|
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NM_021951.2:c.734G>T
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NP_068770.2:p.Gly245Val
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|
XM_006716732.1:c.734G>T
|
XP_006716795.1:p.Gly245Val
|
|
XM_011517770.1:c.782G>T
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XP_011516072.1:p.Gly261Val
|
|
XM_011517771.1:c.782G>T
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XP_011516073.1:p.Gly261Val
|
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XM_011517772.1:c.782G>T
|
XP_011516074.1:p.Gly261Val
|
|
XM_011517773.1:c.260G>T
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XP_011516075.1:p.Gly87Val
|
|
NM_001363767.1:c.260G>T
|
NP_001350696.1:p.Gly87Val
|
|
XM_011517773.3:c.260G>T
|
XP_011516075.1:p.Gly87Val
|
|
XM_017014374.1:c.587-22656G>T
|
XP_016869863.1:n.587-22656G>T
|
|
XM_017014375.1:c.539-22656G>T
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XP_016869864.1:n.539-22656G>T
|
|
XM_024447434.1:c.188G>T
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XP_024303202.1:p.Gly63Val
|
|
NM_021951.3:c.734G>T
MANE Select
|
NP_068770.2:p.Gly245Val
|
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