ENST00000344537.10:c.222G>T
MANE Select
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ENSP00000341680.6:p.Glu74Asp
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ENST00000338950.9:c.222G>T
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ENSP00000344718.5:p.Glu74Asp
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ENST00000344537.9:c.222G>T
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ENSP00000341680.5:p.Glu74Asp
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ENST00000355917.7:c.171G>T
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ENSP00000348183.4:p.Glu57Asp
|
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ENST00000506844.1:c.*220G>T
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ENSP00000424202.1:n.*220G>T
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ENST00000510395.5:c.*132G>T
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ENSP00000424685.1:n.*132G>T
|
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ENST00000511762.2:c.117G>T
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ENSP00000427473.2:p.Glu39Asp
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ENST00000513680.5:c.*220G>T
|
ENSP00000424357.1:n.*220G>T
|
|
ENST00000515875.5:c.171G>T
|
ENSP00000425495.1:p.Glu57Asp
|
|
ENST00000622898.4:c.117G>T
|
ENSP00000481997.1:p.Glu39Asp
|
|
NM_001271667.1:c.-22G>T
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NP_001258596.1:n.-22G>T
|
|
NM_001271668.1:c.171G>T
|
NP_001258597.1:p.Glu57Asp
|
|
NM_001271669.1:c.117G>T
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NP_001258598.1:p.Glu39Asp
|
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NM_032122.4:c.222G>T , LRG_588t1:c.222G>T
|
NP_115498.2:p.Glu74Asp
|
|
NM_183040.2:c.222G>T , LRG_588t2:c.222G>T
|
NP_898861.1:p.Glu74Asp
|
|
NR_036448.1:n.550G>T
|
|
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XM_005249447.3:c.183G>T
|
XP_005249504.1:p.Glu61Asp
|
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XM_011514936.1:c.132G>T
|
XP_011513238.1:p.Glu44Asp
|
|
XM_005249447.4:c.183G>T
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XP_005249504.1:p.Glu61Asp
|
|
XM_011514936.3:c.132G>T
|
XP_011513238.1:p.Glu44Asp
|
|
NM_032122.5:c.222G>T
MANE Select
|
NP_115498.2:p.Glu74Asp
|
|
NR_036448.2:n.520G>T
|
|
|
NM_001271667.2:c.-22G>T
|
NP_001258596.1:n.-22G>T
|
|
NM_001271668.2:c.171G>T
|
NP_001258597.1:p.Glu57Asp
|
|
NM_001271669.2:c.117G>T
|
NP_001258598.1:p.Glu39Asp
|
|
NR_036448.3:n.520G>T
|
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