ENST00000258443.7:c.888C>G
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Gly296=
|
|
ENST00000258443.6:c.888C>G
(EDAR)
|
ENSP00000258443.2:p.Gly296=
|
|
ENST00000376651.1:c.984C>G
(EDAR)
|
ENSP00000365839.1:p.Gly328=
|
|
ENST00000409271.5:c.984C>G
(EDAR)
|
ENSP00000386371.1:p.Gly328=
|
|
NM_022336.3:c.888C>G
(EDAR)
|
NP_071731.1:p.Gly296=
|
|
XM_006712204.1:c.984C>G
(EDAR)
|
XP_006712267.1:p.Gly328=
|
|
XM_011510502.1:c.1035C>G
(EDAR)
|
XP_011508804.1:p.Gly345=
|
|
XM_011510503.1:c.939C>G
(EDAR)
|
XP_011508805.1:p.Gly313=
|
|
XM_011510504.1:c.315C>G
(EDAR)
|
XP_011508806.1:p.Gly105=
|
|
XM_011510502.2:c.1128C>G
(EDAR)
|
XP_011508804.2:p.Gly376=
|
|
XM_011510503.2:c.1032C>G
(EDAR)
|
XP_011508805.2:p.Gly344=
|
|
XM_017004623.2:c.8370+134889G>C
(RANBP2)
|
XP_016860112.1:n.8370+134889G>C
|
|
NM_022336.4:c.888C>G
(EDAR)
MANE Select
|
NP_071731.1:p.Gly296=
|
|