ENST00000258443.7:c.873C>G
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Ala291=
|
|
ENST00000258443.6:c.873C>G
(EDAR)
|
ENSP00000258443.2:p.Ala291=
|
|
ENST00000376651.1:c.969C>G
(EDAR)
|
ENSP00000365839.1:p.Ala323=
|
|
ENST00000409271.5:c.969C>G
(EDAR)
|
ENSP00000386371.1:p.Ala323=
|
|
NM_022336.3:c.873C>G
(EDAR)
|
NP_071731.1:p.Ala291=
|
|
XM_006712204.1:c.969C>G
(EDAR)
|
XP_006712267.1:p.Ala323=
|
|
XM_011510502.1:c.1020C>G
(EDAR)
|
XP_011508804.1:p.Ala340=
|
|
XM_011510503.1:c.924C>G
(EDAR)
|
XP_011508805.1:p.Ala308=
|
|
XM_011510504.1:c.300C>G
(EDAR)
|
XP_011508806.1:p.Ala100=
|
|
XM_011510502.2:c.1113C>G
(EDAR)
|
XP_011508804.2:p.Ala371=
|
|
XM_011510503.2:c.1017C>G
(EDAR)
|
XP_011508805.2:p.Ala339=
|
|
XM_017004623.2:c.8370+134904G>C
(RANBP2)
|
XP_016860112.1:n.8370+134904G>C
|
|
NM_022336.4:c.873C>G
(EDAR)
MANE Select
|
NP_071731.1:p.Ala291=
|
|