ENST00000251810.8:c.111G>T
MANE Select
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ENSP00000251810.3:p.Lys37Asn
|
|
ENST00000251810.7:c.111G>T
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ENSP00000251810.3:p.Lys37Asn
|
|
ENST00000395912.6:c.49-6208G>T
|
ENSP00000379248.2:n.49-6208G>T
|
|
ENST00000517517.1:n.420G>T
|
|
|
ENST00000519317.5:c.48+6585G>T
|
ENSP00000430641.1:n.48+6585G>T
|
|
ENST00000519962.5:c.48+6585G>T
|
ENSP00000429140.1:n.48+6585G>T
|
|
ENST00000522368.5:c.280G>T
|
|
|
ENST00000522394.1:c.111G>T
|
ENSP00000429578.1:p.Lys37Asn
|
|
ENST00000523957.1:c.*34G>T
|
ENSP00000427830.1:n.*34G>T
|
|
ENST00000621845.1:c.-52G>T
|
ENSP00000484318.1:n.-52G>T
|
|
NM_001172477.1:c.327G>T , LRG_788t1:c.327G>T
|
NP_001165948.1:p.Lys109Asn
|
|
NM_001172478.1:c.49-6208G>T
|
NP_001165949.1:n.49-6208G>T
|
|
NM_015713.4:c.111G>T , LRG_788t2:c.111G>T
|
NP_056528.2:p.Lys37Asn
|
|
NM_001172478.2:c.49-6208G>T
|
NP_001165949.1:n.49-6208G>T
|
|
NM_015713.5:c.111G>T
MANE Select
|
NP_056528.2:p.Lys37Asn
|
|