ENST00000251810.8:c.1037C>G
MANE Select
|
ENSP00000251810.3:p.Thr346Ser
|
|
ENST00000251810.7:c.1037C>G
|
ENSP00000251810.3:p.Thr346Ser
|
|
ENST00000395910.6:n.424C>G
|
|
|
ENST00000395912.6:c.881C>G
|
ENSP00000379248.2:p.Thr294Ser
|
|
ENST00000519317.5:c.401C>G
|
ENSP00000430641.1:p.Thr134Ser
|
|
ENST00000519962.5:c.182C>G
|
ENSP00000429140.1:p.Thr61Ser
|
|
ENST00000522368.5:c.1206C>G
|
|
|
ENST00000522394.1:c.370C>G
|
ENSP00000429578.1:n.370C>G
|
|
ENST00000621845.1:c.875C>G
|
ENSP00000484318.1:p.Thr292Ser
|
|
NM_001172477.1:c.1253C>G , LRG_788t1:c.1253C>G
|
NP_001165948.1:p.Thr418Ser
|
|
NM_001172478.1:c.881C>G
|
NP_001165949.1:p.Thr294Ser
|
|
NM_015713.4:c.1037C>G , LRG_788t2:c.1037C>G
|
NP_056528.2:p.Thr346Ser
|
|
NM_001172478.2:c.881C>G
|
NP_001165949.1:p.Thr294Ser
|
|
NM_015713.5:c.1037C>G
MANE Select
|
NP_056528.2:p.Thr346Ser
|
|