ENST00000327047.6:c.412T=
MANE Select
|
ENSP00000322280.1:p.Tyr138=
|
|
ENST00000468836.2:c.560T=
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ENSP00000419892.2:n.560T=
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|
ENST00000644099.1:c.404T=
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ENSP00000494762.1:n.404T=
|
|
ENST00000295911.6:c.184T=
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ENSP00000295911.2:p.Tyr62=
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|
ENST00000327047.5:c.412T=
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ENSP00000322280.1:p.Tyr138=
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|
ENST00000328863.8:c.412T=
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ENSP00000329158.4:p.Tyr138=
|
|
ENST00000468836.1:c.184T=
|
ENSP00000419892.1:p.Tyr62=
|
|
ENST00000472224.1:n.418T=
|
|
|
ENST00000485607.1:c.76T=
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ENSP00000419244.1:p.Tyr26=
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|
ENST00000562308.5:c.83T=
|
|
|
ENST00000565169.1:c.141T=
|
|
|
ENST00000569170.5:c.141T=
|
|
|
NM_001195794.1:c.412T= , LRG_700t1:c.412T=
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NP_001182723.1:p.Tyr138=
|
|
NM_001256819.1:c.*26T=
|
NP_001243748.1:n.*26T=
|
|
NM_052995.2:c.184T= , LRG_700t2:c.184T=
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NP_443721.1:p.Tyr62=
|
|
NM_174878.2:c.412T=
|
NP_777367.1:p.Tyr138=
|
|
NR_046380.2:n.854T=
|
|
|
XR_924167.1:n.724T=
|
|
|
NM_001256819.2:c.*26T=
|
NP_001243748.1:n.*26T=
|
|
NM_174878.3:c.412T=
MANE Select
|
NP_777367.1:p.Tyr138=
|
|
NR_046380.3:n.582T=
|
|
|