ENST00000327047.6:c.404T>G
MANE Select
|
ENSP00000322280.1:p.Leu135Arg
|
|
ENST00000468836.2:c.552T>G
|
ENSP00000419892.2:n.552T>G
|
|
ENST00000644099.1:c.396T>G
|
ENSP00000494762.1:n.396T>G
|
|
ENST00000295911.6:c.176T>G
|
ENSP00000295911.2:p.Leu59Arg
|
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ENST00000327047.5:c.404T>G
|
ENSP00000322280.1:p.Leu135Arg
|
|
ENST00000328863.8:c.404T>G
|
ENSP00000329158.4:p.Leu135Arg
|
|
ENST00000468836.1:c.176T>G
|
ENSP00000419892.1:p.Leu59Arg
|
|
ENST00000472224.1:n.410T>G
|
|
|
ENST00000485607.1:c.68T>G
|
ENSP00000419244.1:p.Leu23Arg
|
|
ENST00000562308.5:c.75T>G
|
|
|
ENST00000565169.1:c.133T>G
|
|
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ENST00000569170.5:c.133T>G
|
|
|
NM_001195794.1:c.404T>G , LRG_700t1:c.404T>G
|
NP_001182723.1:p.Leu135Arg
|
|
NM_001256819.1:c.*18T>G
|
NP_001243748.1:n.*18T>G
|
|
NM_052995.2:c.176T>G , LRG_700t2:c.176T>G
|
NP_443721.1:p.Leu59Arg
|
|
NM_174878.2:c.404T>G
|
NP_777367.1:p.Leu135Arg
|
|
NR_046380.2:n.846T>G
|
|
|
XR_924167.1:n.716T>G
|
|
|
NM_001256819.2:c.*18T>G
|
NP_001243748.1:n.*18T>G
|
|
NM_174878.3:c.404T>G
MANE Select
|
NP_777367.1:p.Leu135Arg
|
|
NR_046380.3:n.574T>G
|
|
|