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NM_002168.4:c.266G>A
MANE Select
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NP_002159.2:p.Arg89His
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ENST00000330062.8:c.266G>A
MANE Select
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ENSP00000331897.4:p.Arg89His
|
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NM_001289910.1:c.110G>A , LRG_611t1:c.110G>A
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NP_001276839.1:p.Arg37His
|
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NM_001290114.1:c.-17-1839G>A
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NP_001277043.1:n.-17-1839G>A
|
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NM_001290114.2:c.-17-1839G>A
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NP_001277043.1:n.-17-1839G>A
|
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NM_002168.3:c.266G>A , LRG_611t2:c.266G>A
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NP_002159.2:p.Arg89His
|
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ENST00000330062.7:c.266G>A
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ENSP00000331897.3:p.Arg89His
|
|
ENST00000540499.2:c.110G>A
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ENSP00000446147.2:p.Arg37His
|
|
ENST00000559482.5:c.207+967G>A
|
ENSP00000453016.1:n.207+967G>A
|
|
ENST00000560061.1:c.116-1839G>A
|
ENSP00000453254.1:n.116-1839G>A
|