ENST00000373366.3:c.57G>T
(GJB3)
MANE Select
|
ENSP00000362464.2:p.Ala19=
|
|
ENST00000373362.3:c.57G>T
(GJB3)
|
ENSP00000362460.3:p.Ala19=
|
|
ENST00000373366.2:c.57G>T
(GJB3)
|
ENSP00000362464.2:p.Ala19=
|
|
ENST00000426886.1:c.208-66410C>A
(SMIM12)
|
ENSP00000429902.1:n.208-66410C>A
|
|
NM_001005752.1:c.57G>T
(GJB3)
|
NP_001005752.1:p.Ala19=
|
|
NM_024009.2:c.57G>T
(GJB3)
|
NP_076872.1:p.Ala19=
|
|
XR_947179.1:n.1001+13552C>A
|
|
|
XR_001737967.1:n.1023+13552C>A
|
|
|
NM_024009.3:c.57G>T
(GJB3)
MANE Select
|
NP_076872.1:p.Ala19=
|
|
NM_001005752.2:c.57G>T
(GJB3)
|
NP_001005752.1:p.Ala19=
|
|