ENST00000251810.8:c.1039T>C
MANE Select
|
ENSP00000251810.3:p.Leu347=
|
|
ENST00000251810.7:c.1039T>C
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ENSP00000251810.3:p.Leu347=
|
|
ENST00000395910.6:n.426T>C
|
|
|
ENST00000395912.6:c.883T>C
|
ENSP00000379248.2:p.Leu295=
|
|
ENST00000519317.5:c.403T>C
|
ENSP00000430641.1:p.Leu135=
|
|
ENST00000519962.5:c.184T>C
|
ENSP00000429140.1:p.Leu62=
|
|
ENST00000522368.5:c.1208T>C
|
|
|
ENST00000522394.1:c.372T>C
|
ENSP00000429578.1:n.372T>C
|
|
ENST00000621845.1:c.877T>C
|
ENSP00000484318.1:p.Leu293=
|
|
NM_001172477.1:c.1255T>C , LRG_788t1:c.1255T>C
|
NP_001165948.1:p.Leu419=
|
|
NM_001172478.1:c.883T>C
|
NP_001165949.1:p.Leu295=
|
|
NM_015713.4:c.1039T>C , LRG_788t2:c.1039T>C
|
NP_056528.2:p.Leu347=
|
|
NM_001172478.2:c.883T>C
|
NP_001165949.1:p.Leu295=
|
|
NM_015713.5:c.1039T>C
MANE Select
|
NP_056528.2:p.Leu347=
|
|