ENST00000251810.8:c.344T>G
MANE Select
|
ENSP00000251810.3:p.Val115Gly
|
|
ENST00000251810.7:c.344T>G
|
ENSP00000251810.3:p.Val115Gly
|
|
ENST00000395912.6:c.188T>G
|
ENSP00000379248.2:p.Val63Gly
|
|
ENST00000519317.5:c.49-10838T>G
|
ENSP00000430641.1:n.49-10838T>G
|
|
ENST00000519962.5:c.48+13831T>G
|
ENSP00000429140.1:n.48+13831T>G
|
|
ENST00000522368.5:c.513T>G
|
|
|
ENST00000522394.1:c.122+7235T>G
|
ENSP00000429578.1:n.122+7235T>G
|
|
ENST00000523957.1:c.*267T>G
|
ENSP00000427830.1:n.*267T>G
|
|
ENST00000621845.1:c.182T>G
|
ENSP00000484318.1:p.Val61Gly
|
|
NM_001172477.1:c.560T>G , LRG_788t1:c.560T>G
|
NP_001165948.1:p.Val187Gly
|
|
NM_001172478.1:c.188T>G
|
NP_001165949.1:p.Val63Gly
|
|
NM_015713.4:c.344T>G , LRG_788t2:c.344T>G
|
NP_056528.2:p.Val115Gly
|
|
NM_001172478.2:c.188T>G
|
NP_001165949.1:p.Val63Gly
|
|
NM_015713.5:c.344T>G
MANE Select
|
NP_056528.2:p.Val115Gly
|
|