|
ENST00000258443.7:c.948C>T
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Ser316=
|
|
|
ENST00000258443.6:c.948C>T
(EDAR)
|
ENSP00000258443.2:p.Ser316=
|
|
|
ENST00000376651.1:c.1044C>T
(EDAR)
|
ENSP00000365839.1:p.Ser348=
|
|
|
ENST00000409271.5:c.1044C>T
(EDAR)
|
ENSP00000386371.1:p.Ser348=
|
|
|
NM_022336.3:c.948C>T
(EDAR)
|
NP_071731.1:p.Ser316=
|
|
|
XM_006712204.1:c.1044C>T
(EDAR)
|
XP_006712267.1:p.Ser348=
|
|
|
XM_011510502.1:c.1095C>T
(EDAR)
|
XP_011508804.1:p.Ser365=
|
|
|
XM_011510503.1:c.999C>T
(EDAR)
|
XP_011508805.1:p.Ser333=
|
|
|
XM_011510504.1:c.375C>T
(EDAR)
|
XP_011508806.1:p.Ser125=
|
|
|
XM_011510502.2:c.1188C>T
(EDAR)
|
XP_011508804.2:p.Ser396=
|
|
|
XM_011510503.2:c.1092C>T
(EDAR)
|
XP_011508805.2:p.Ser364=
|
|
|
XM_017004623.2:c.8370+134829G>A
(RANBP2)
|
XP_016860112.1:n.8370+134829G>A
|
|
|
NM_022336.4:c.948C>T
(EDAR)
MANE Select
|
NP_071731.1:p.Ser316=
|
|
