ENST00000261304.7:c.657G>C
MANE Select
|
ENSP00000261304.2:p.Gln219His
|
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ENST00000261304.6:c.657G>C
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ENSP00000261304.2:p.Gln219His
|
|
ENST00000393568.8:c.588G>C
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ENSP00000377198.4:p.Gln196His
|
|
ENST00000393569.6:c.579G>C
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ENSP00000377199.2:p.Gln193His
|
|
ENST00000474294.6:n.647G>C
|
|
|
ENST00000477716.3:n.412G>C
|
|
|
ENST00000544807.6:c.489G>C
|
ENSP00000437513.2:p.Gln163His
|
|
ENST00000554916.5:n.536G>C
|
|
|
ENST00000555000.5:c.24G>C
|
ENSP00000450472.1:p.Gln8His
|
|
ENST00000557316.5:c.*55G>C
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ENSP00000452314.1:n.*55G>C
|
|
ENST00000622264.4:c.647G>C
|
|
|
NM_000153.3:c.657G>C
|
NP_000144.2:p.Gln219His
|
|
NM_001201401.1:c.588G>C
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NP_001188330.1:p.Gln196His
|
|
NM_001201402.1:c.579G>C
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NP_001188331.1:p.Gln193His
|
|
XM_011536618.1:c.489G>C
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XP_011534920.1:p.Gln163His
|
|
XM_011536618.2:c.489G>C
|
XP_011534920.1:p.Gln163His
|
|
NM_000153.4:c.657G>C
MANE Select
|
NP_000144.2:p.Gln219His
|
|
NM_001201401.2:c.588G>C
|
NP_001188330.1:p.Gln196His
|
|
NM_001201402.2:c.579G>C
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NP_001188331.1:p.Gln193His
|
|