ENST00000336906.6:c.102T>G
MANE Select
|
ENSP00000338082.4:p.Val34=
|
|
ENST00000380252.6:c.-64T>G
|
ENSP00000369602.2:n.-64T>G
|
|
ENST00000380259.7:c.1648T>G
|
ENSP00000369609.3:n.1648T>G
|
|
ENST00000642908.1:c.102T>G
|
ENSP00000495346.1:p.Val34=
|
|
ENST00000647543.1:c.102T>G
|
ENSP00000496470.1:p.Val34=
|
|
ENST00000336906.4:c.102T>G
|
ENSP00000338082.4:p.Val34=
|
|
ENST00000380252.5:c.72T>G
|
ENSP00000369602.1:p.Val24=
|
|
ENST00000380259.6:c.102T>G
|
ENSP00000369609.2:p.Val34=
|
|
ENST00000444587.1:c.64T>G
|
ENSP00000488218.1:p.Cys22Gly
|
|
ENST00000620888.4:c.102T>G
|
ENSP00000479637.1:p.Val34=
|
|
ENST00000624109.1:c.253A>C
|
ENSP00000485458.1:p.Asn85His
|
|
NM_000184.2:c.102T>G
|
NP_000175.1:p.Val34=
|
|
NM_000184.3:c.102T>G
MANE Select
|
NP_000175.1:p.Val34=
|
|