ENST00000258443.7:c.907C>T
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Leu303=
|
|
ENST00000258443.6:c.907C>T
(EDAR)
|
ENSP00000258443.2:p.Leu303=
|
|
ENST00000376651.1:c.1003C>T
(EDAR)
|
ENSP00000365839.1:p.Leu335=
|
|
ENST00000409271.5:c.1003C>T
(EDAR)
|
ENSP00000386371.1:p.Leu335=
|
|
NM_022336.3:c.907C>T
(EDAR)
|
NP_071731.1:p.Leu303=
|
|
XM_006712204.1:c.1003C>T
(EDAR)
|
XP_006712267.1:p.Leu335=
|
|
XM_011510502.1:c.1054C>T
(EDAR)
|
XP_011508804.1:p.Leu352=
|
|
XM_011510503.1:c.958C>T
(EDAR)
|
XP_011508805.1:p.Leu320=
|
|
XM_011510504.1:c.334C>T
(EDAR)
|
XP_011508806.1:p.Leu112=
|
|
XM_011510502.2:c.1147C>T
(EDAR)
|
XP_011508804.2:p.Leu383=
|
|
XM_011510503.2:c.1051C>T
(EDAR)
|
XP_011508805.2:p.Leu351=
|
|
XM_017004623.2:c.8370+134870G>A
(RANBP2)
|
XP_016860112.1:n.8370+134870G>A
|
|
NM_022336.4:c.907C>T
(EDAR)
MANE Select
|
NP_071731.1:p.Leu303=
|
|