|
ENST00000258443.7:c.1167G>T
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Gly389=
|
|
|
ENST00000258443.6:c.1167G>T
(EDAR)
|
ENSP00000258443.2:p.Gly389=
|
|
|
ENST00000376651.1:c.1263G>T
(EDAR)
|
ENSP00000365839.1:p.Gly421=
|
|
|
ENST00000409271.5:c.1263G>T
(EDAR)
|
ENSP00000386371.1:p.Gly421=
|
|
|
NM_022336.3:c.1167G>T
(EDAR)
|
NP_071731.1:p.Gly389=
|
|
|
XM_006712204.1:c.1263G>T
(EDAR)
|
XP_006712267.1:p.Gly421=
|
|
|
XM_011510502.1:c.1314G>T
(EDAR)
|
XP_011508804.1:p.Gly438=
|
|
|
XM_011510503.1:c.1218G>T
(EDAR)
|
XP_011508805.1:p.Gly406=
|
|
|
XM_011510504.1:c.594G>T
(EDAR)
|
XP_011508806.1:p.Gly198=
|
|
|
XM_011510502.2:c.1407G>T
(EDAR)
|
XP_011508804.2:p.Gly469=
|
|
|
XM_011510503.2:c.1311G>T
(EDAR)
|
XP_011508805.2:p.Gly437=
|
|
|
XM_017004623.2:c.8370+124041C>A
(RANBP2)
|
XP_016860112.1:n.8370+124041C>A
|
|
|
NM_022336.4:c.1167G>T
(EDAR)
MANE Select
|
NP_071731.1:p.Gly389=
|
|
