ENST00000258443.7:c.1112T>G
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Val371Gly
|
|
ENST00000258443.6:c.1112T>G
(EDAR)
|
ENSP00000258443.2:p.Val371Gly
|
|
ENST00000376651.1:c.1208T>G
(EDAR)
|
ENSP00000365839.1:p.Val403Gly
|
|
ENST00000409271.5:c.1208T>G
(EDAR)
|
ENSP00000386371.1:p.Val403Gly
|
|
NM_022336.3:c.1112T>G
(EDAR)
|
NP_071731.1:p.Val371Gly
|
|
XM_006712204.1:c.1208T>G
(EDAR)
|
XP_006712267.1:p.Val403Gly
|
|
XM_011510502.1:c.1259T>G
(EDAR)
|
XP_011508804.1:p.Val420Gly
|
|
XM_011510503.1:c.1163T>G
(EDAR)
|
XP_011508805.1:p.Val388Gly
|
|
XM_011510504.1:c.539T>G
(EDAR)
|
XP_011508806.1:p.Val180Gly
|
|
XM_011510502.2:c.1352T>G
(EDAR)
|
XP_011508804.2:p.Val451Gly
|
|
XM_011510503.2:c.1256T>G
(EDAR)
|
XP_011508805.2:p.Val419Gly
|
|
XM_017004623.2:c.8370+124096A>C
(RANBP2)
|
XP_016860112.1:n.8370+124096A>C
|
|
NM_022336.4:c.1112T>G
(EDAR)
MANE Select
|
NP_071731.1:p.Val371Gly
|
|