ENST00000258443.7:c.942C>G
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Ala314=
|
|
ENST00000258443.6:c.942C>G
(EDAR)
|
ENSP00000258443.2:p.Ala314=
|
|
ENST00000376651.1:c.1038C>G
(EDAR)
|
ENSP00000365839.1:p.Ala346=
|
|
ENST00000409271.5:c.1038C>G
(EDAR)
|
ENSP00000386371.1:p.Ala346=
|
|
NM_022336.3:c.942C>G
(EDAR)
|
NP_071731.1:p.Ala314=
|
|
XM_006712204.1:c.1038C>G
(EDAR)
|
XP_006712267.1:p.Ala346=
|
|
XM_011510502.1:c.1089C>G
(EDAR)
|
XP_011508804.1:p.Ala363=
|
|
XM_011510503.1:c.993C>G
(EDAR)
|
XP_011508805.1:p.Ala331=
|
|
XM_011510504.1:c.369C>G
(EDAR)
|
XP_011508806.1:p.Ala123=
|
|
XM_011510502.2:c.1182C>G
(EDAR)
|
XP_011508804.2:p.Ala394=
|
|
XM_011510503.2:c.1086C>G
(EDAR)
|
XP_011508805.2:p.Ala362=
|
|
XM_017004623.2:c.8370+134835G>C
(RANBP2)
|
XP_016860112.1:n.8370+134835G>C
|
|
NM_022336.4:c.942C>G
(EDAR)
MANE Select
|
NP_071731.1:p.Ala314=
|
|