ENST00000258443.7:c.1314G>C
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Val438=
|
|
ENST00000258443.6:c.1314G>C
(EDAR)
|
ENSP00000258443.2:p.Val438=
|
|
ENST00000376651.1:c.1410G>C
(EDAR)
|
ENSP00000365839.1:p.Val470=
|
|
ENST00000409271.5:c.1410G>C
(EDAR)
|
ENSP00000386371.1:p.Val470=
|
|
NM_022336.3:c.1314G>C
(EDAR)
|
NP_071731.1:p.Val438=
|
|
XM_006712204.1:c.1410G>C
(EDAR)
|
XP_006712267.1:p.Val470=
|
|
XM_011510502.1:c.1461G>C
(EDAR)
|
XP_011508804.1:p.Val487=
|
|
XM_011510503.1:c.1365G>C
(EDAR)
|
XP_011508805.1:p.Val455=
|
|
XM_011510504.1:c.741G>C
(EDAR)
|
XP_011508806.1:p.Val247=
|
|
XM_011510502.2:c.1554G>C
(EDAR)
|
XP_011508804.2:p.Val518=
|
|
XM_011510503.2:c.1458G>C
(EDAR)
|
XP_011508805.2:p.Val486=
|
|
XM_017004623.2:c.8370+123894C>G
(RANBP2)
|
XP_016860112.1:n.8370+123894C>G
|
|
NM_022336.4:c.1314G>C
(EDAR)
MANE Select
|
NP_071731.1:p.Val438=
|
|