ENST00000336906.6:c.123G>A
MANE Select
|
ENSP00000338082.4:p.Arg41=
|
|
ENST00000380252.6:c.-43G>A
|
ENSP00000369602.2:n.-43G>A
|
|
ENST00000380259.7:c.1669G>A
|
ENSP00000369609.3:n.1669G>A
|
|
ENST00000642908.1:c.123G>A
|
ENSP00000495346.1:p.Arg41=
|
|
ENST00000647543.1:c.123G>A
|
ENSP00000496470.1:p.Arg41=
|
|
ENST00000336906.4:c.123G>A
|
ENSP00000338082.4:p.Arg41=
|
|
ENST00000380252.5:c.93G>A
|
ENSP00000369602.1:p.Arg31=
|
|
ENST00000380259.6:c.123G>A
|
ENSP00000369609.2:p.Arg41=
|
|
ENST00000444587.1:c.85G>A
|
ENSP00000488218.1:p.Val29Ile
|
|
ENST00000620888.4:c.123G>A
|
ENSP00000479637.1:p.Arg41=
|
|
ENST00000624109.1:c.232C>T
|
ENSP00000485458.1:p.Pro78Ser
|
|
NM_000184.2:c.123G>A
|
NP_000175.1:p.Arg41=
|
|
NM_000184.3:c.123G>A
MANE Select
|
NP_000175.1:p.Arg41=
|
|