ENST00000704074.1:c.46A>T
|
|
|
ENST00000283179.14:c.368A>T
|
ENSP00000283179.10:p.Glu123Val
|
|
ENST00000444376.7:c.368A>T
|
ENSP00000393151.2:p.Glu123Val
|
|
ENST00000476241.2:n.553A>T
|
|
|
ENST00000638475.1:c.152A>T
|
ENSP00000491305.1:p.Glu51Val
|
|
ENST00000638952.1:n.599A>T
|
|
|
ENST00000640218.2:c.368A>T
MANE Select
|
ENSP00000491215.1:p.Glu123Val
|
|
ENST00000640306.1:c.368A>T
|
ENSP00000491685.1:p.Glu123Val
|
|
ENST00000640440.1:c.68A>T
|
ENSP00000491263.1:p.Glu23Val
|
|
ENST00000649899.1:n.592A>T
|
|
|
ENST00000283179.13:c.368A>T
|
ENSP00000283179.9:p.Glu123Val
|
|
ENST00000444376.6:c.368A>T
|
ENSP00000393151.2:p.Glu123Val
|
|
ENST00000476241.1:n.552A>T
|
|
|
NM_004501.3:c.368A>T
|
NP_004492.2:p.Glu123Val
|
|
NM_031844.2:c.368A>T
|
NP_114032.2:p.Glu123Val
|
|
NM_031844.3:c.368A>T
MANE Select
|
NP_114032.2:p.Glu123Val
|
|