ENST00000258443.7:c.894G>T
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Pro298=
|
|
ENST00000258443.6:c.894G>T
(EDAR)
|
ENSP00000258443.2:p.Pro298=
|
|
ENST00000376651.1:c.990G>T
(EDAR)
|
ENSP00000365839.1:p.Pro330=
|
|
ENST00000409271.5:c.990G>T
(EDAR)
|
ENSP00000386371.1:p.Pro330=
|
|
NM_022336.3:c.894G>T
(EDAR)
|
NP_071731.1:p.Pro298=
|
|
XM_006712204.1:c.990G>T
(EDAR)
|
XP_006712267.1:p.Pro330=
|
|
XM_011510502.1:c.1041G>T
(EDAR)
|
XP_011508804.1:p.Pro347=
|
|
XM_011510503.1:c.945G>T
(EDAR)
|
XP_011508805.1:p.Pro315=
|
|
XM_011510504.1:c.321G>T
(EDAR)
|
XP_011508806.1:p.Pro107=
|
|
XM_011510502.2:c.1134G>T
(EDAR)
|
XP_011508804.2:p.Pro378=
|
|
XM_011510503.2:c.1038G>T
(EDAR)
|
XP_011508805.2:p.Pro346=
|
|
XM_017004623.2:c.8370+134883C>A
(RANBP2)
|
XP_016860112.1:n.8370+134883C>A
|
|
NM_022336.4:c.894G>T
(EDAR)
MANE Select
|
NP_071731.1:p.Pro298=
|
|