ENST00000251810.8:c.1038C=
MANE Select
|
ENSP00000251810.3:p.Thr346=
|
|
ENST00000251810.7:c.1038C=
|
ENSP00000251810.3:p.Thr346=
|
|
ENST00000395910.6:n.425C=
|
|
|
ENST00000395912.6:c.882C=
|
ENSP00000379248.2:p.Thr294=
|
|
ENST00000519317.5:c.402C=
|
ENSP00000430641.1:p.Thr134=
|
|
ENST00000519962.5:c.183C=
|
ENSP00000429140.1:p.Thr61=
|
|
ENST00000522368.5:c.1207C=
|
|
|
ENST00000522394.1:c.371C=
|
ENSP00000429578.1:n.371C=
|
|
ENST00000621845.1:c.876C=
|
ENSP00000484318.1:p.Thr292=
|
|
NM_001172477.1:c.1254C= , LRG_788t1:c.1254C=
|
NP_001165948.1:p.Thr418=
|
|
NM_001172478.1:c.882C=
|
NP_001165949.1:p.Thr294=
|
|
NM_015713.4:c.1038C= , LRG_788t2:c.1038C=
|
NP_056528.2:p.Thr346=
|
|
NM_001172478.2:c.882C=
|
NP_001165949.1:p.Thr294=
|
|
NM_015713.5:c.1038C=
MANE Select
|
NP_056528.2:p.Thr346=
|
|