ENST00000251810.8:c.1019C>T
MANE Select
|
ENSP00000251810.3:p.Thr340Ile
|
|
ENST00000251810.7:c.1019C>T
|
ENSP00000251810.3:p.Thr340Ile
|
|
ENST00000395910.6:n.406C>T
|
|
|
ENST00000395912.6:c.863C>T
|
ENSP00000379248.2:p.Thr288Ile
|
|
ENST00000519317.5:c.383C>T
|
ENSP00000430641.1:p.Thr128Ile
|
|
ENST00000519962.5:c.164C>T
|
ENSP00000429140.1:p.Thr55Ile
|
|
ENST00000522368.5:c.1188C>T
|
|
|
ENST00000522394.1:c.352C>T
|
ENSP00000429578.1:n.352C>T
|
|
ENST00000621845.1:c.857C>T
|
ENSP00000484318.1:p.Thr286Ile
|
|
NM_001172477.1:c.1235C>T , LRG_788t1:c.1235C>T
|
NP_001165948.1:p.Thr412Ile
|
|
NM_001172478.1:c.863C>T
|
NP_001165949.1:p.Thr288Ile
|
|
NM_015713.4:c.1019C>T , LRG_788t2:c.1019C>T
|
NP_056528.2:p.Thr340Ile
|
|
NM_001172478.2:c.863C>T
|
NP_001165949.1:p.Thr288Ile
|
|
NM_015713.5:c.1019C>T
MANE Select
|
NP_056528.2:p.Thr340Ile
|
|