ENST00000258443.7:c.859G>A
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Asp287Asn
|
|
ENST00000258443.6:c.859G>A
(EDAR)
|
ENSP00000258443.2:p.Asp287Asn
|
|
ENST00000376651.1:c.955G>A
(EDAR)
|
ENSP00000365839.1:p.Asp319Asn
|
|
ENST00000409271.5:c.955G>A
(EDAR)
|
ENSP00000386371.1:p.Asp319Asn
|
|
NM_022336.3:c.859G>A
(EDAR)
|
NP_071731.1:p.Asp287Asn
|
|
XM_006712204.1:c.955G>A
(EDAR)
|
XP_006712267.1:p.Asp319Asn
|
|
XM_011510502.1:c.1006G>A
(EDAR)
|
XP_011508804.1:p.Asp336Asn
|
|
XM_011510503.1:c.910G>A
(EDAR)
|
XP_011508805.1:p.Asp304Asn
|
|
XM_011510504.1:c.286G>A
(EDAR)
|
XP_011508806.1:p.Asp96Asn
|
|
XM_011510502.2:c.1099G>A
(EDAR)
|
XP_011508804.2:p.Asp367Asn
|
|
XM_011510503.2:c.1003G>A
(EDAR)
|
XP_011508805.2:p.Asp335Asn
|
|
XM_017004623.2:c.8370+134918C>T
(RANBP2)
|
XP_016860112.1:n.8370+134918C>T
|
|
NM_022336.4:c.859G>A
(EDAR)
MANE Select
|
NP_071731.1:p.Asp287Asn
|
|