ENST00000369689.6:c.291A>T
MANE Select
|
ENSP00000358703.1:p.Glu97Asp
|
|
ENST00000369687.2:c.117A>T
|
ENSP00000358701.1:p.Glu39Asp
|
|
ENST00000369689.5:c.291A>T
|
ENSP00000358703.1:p.Glu97Asp
|
|
ENST00000635617.1:n.3704A>T
|
|
|
NM_001009994.2:c.291A>T
|
NP_001009994.1:p.Glu97Asp
|
|
NR_103525.1:n.348A>T
|
|
|
NR_103525.2:n.286A>T
|
|
|
NM_001009994.3:c.291A>T
MANE Select
|
NP_001009994.1:p.Glu97Asp
|
|
NM_001400774.1:c.-28+3132A>T
|
NP_001387703.1:n.-28+3132A>T
|
|
NM_001400899.1:c.354A>T
|
NP_001387828.1:p.Glu118Asp
|
|
NM_001400900.1:c.*3128A>T
|
NP_001387829.1:n.*3128A>T
|
|
NR_174603.1:n.234+3132A>T
|
|
|
NR_174604.1:n.296+3132A>T
|
|
|
NR_174605.1:n.455+3234A>T
|
|
|
NR_174622.1:n.3366A>T
|
|
|