ENST00000258443.7:c.1336G>T
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Ala446Ser
|
|
ENST00000258443.6:c.1336G>T
(EDAR)
|
ENSP00000258443.2:p.Ala446Ser
|
|
ENST00000376651.1:c.1432G>T
(EDAR)
|
ENSP00000365839.1:p.Ala478Ser
|
|
ENST00000409271.5:c.1432G>T
(EDAR)
|
ENSP00000386371.1:p.Ala478Ser
|
|
NM_022336.3:c.1336G>T
(EDAR)
|
NP_071731.1:p.Ala446Ser
|
|
XM_006712204.1:c.1432G>T
(EDAR)
|
XP_006712267.1:p.Ala478Ser
|
|
XM_011510502.1:c.1483G>T
(EDAR)
|
XP_011508804.1:p.Ala495Ser
|
|
XM_011510503.1:c.1387G>T
(EDAR)
|
XP_011508805.1:p.Ala463Ser
|
|
XM_011510504.1:c.763G>T
(EDAR)
|
XP_011508806.1:p.Ala255Ser
|
|
XM_011510502.2:c.1576G>T
(EDAR)
|
XP_011508804.2:p.Ala526Ser
|
|
XM_011510503.2:c.1480G>T
(EDAR)
|
XP_011508805.2:p.Ala494Ser
|
|
XM_017004623.2:c.8370+123872C>A
(RANBP2)
|
XP_016860112.1:n.8370+123872C>A
|
|
NM_022336.4:c.1336G>T
(EDAR)
MANE Select
|
NP_071731.1:p.Ala446Ser
|
|