ENST00000327047.6:c.412T>C
MANE Select
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ENSP00000322280.1:p.Tyr138His
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ENST00000468836.2:c.560T>C
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ENSP00000419892.2:n.560T>C
|
|
ENST00000644099.1:c.404T>C
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ENSP00000494762.1:n.404T>C
|
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ENST00000295911.6:c.184T>C
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ENSP00000295911.2:p.Tyr62His
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ENST00000327047.5:c.412T>C
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ENSP00000322280.1:p.Tyr138His
|
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ENST00000328863.8:c.412T>C
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ENSP00000329158.4:p.Tyr138His
|
|
ENST00000468836.1:c.184T>C
|
ENSP00000419892.1:p.Tyr62His
|
|
ENST00000472224.1:n.418T>C
|
|
|
ENST00000485607.1:c.76T>C
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ENSP00000419244.1:p.Tyr26His
|
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ENST00000562308.5:c.83T>C
|
|
|
ENST00000565169.1:c.141T>C
|
|
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ENST00000569170.5:c.141T>C
|
|
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NM_001195794.1:c.412T>C , LRG_700t1:c.412T>C
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NP_001182723.1:p.Tyr138His
|
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NM_001256819.1:c.*26T>C
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NP_001243748.1:n.*26T>C
|
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NM_052995.2:c.184T>C , LRG_700t2:c.184T>C
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NP_443721.1:p.Tyr62His
|
|
NM_174878.2:c.412T>C
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NP_777367.1:p.Tyr138His
|
|
NR_046380.2:n.854T>C
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|
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XR_924167.1:n.724T>C
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|
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NM_001256819.2:c.*26T>C
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NP_001243748.1:n.*26T>C
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|
NM_174878.3:c.412T>C
MANE Select
|
NP_777367.1:p.Tyr138His
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NR_046380.3:n.582T>C
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|
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