ENST00000251810.8:c.1023A>C
MANE Select
|
ENSP00000251810.3:p.Thr341=
|
|
ENST00000251810.7:c.1023A>C
|
ENSP00000251810.3:p.Thr341=
|
|
ENST00000395910.6:n.410A>C
|
|
|
ENST00000395912.6:c.867A>C
|
ENSP00000379248.2:p.Thr289=
|
|
ENST00000519317.5:c.387A>C
|
ENSP00000430641.1:p.Thr129=
|
|
ENST00000519962.5:c.168A>C
|
ENSP00000429140.1:p.Thr56=
|
|
ENST00000522368.5:c.1192A>C
|
|
|
ENST00000522394.1:c.356A>C
|
ENSP00000429578.1:n.356A>C
|
|
ENST00000621845.1:c.861A>C
|
ENSP00000484318.1:p.Thr287=
|
|
NM_001172477.1:c.1239A>C , LRG_788t1:c.1239A>C
|
NP_001165948.1:p.Thr413=
|
|
NM_001172478.1:c.867A>C
|
NP_001165949.1:p.Thr289=
|
|
NM_015713.4:c.1023A>C , LRG_788t2:c.1023A>C
|
NP_056528.2:p.Thr341=
|
|
NM_001172478.2:c.867A>C
|
NP_001165949.1:p.Thr289=
|
|
NM_015713.5:c.1023A>C
MANE Select
|
NP_056528.2:p.Thr341=
|
|