ENST00000580223.2:c.-308A>T
(OTOP2)
|
ENSP00000463837.2:n.-308A>T
|
|
ENST00000614341.5:c.117T>A
(USH1G)
MANE Select
|
ENSP00000480279.1:p.Ala39=
|
|
ENST00000579243.1:c.117T>A
(USH1G)
|
ENSP00000462568.1:p.Ala39=
|
|
ENST00000614341.4:c.117T>A
(USH1G)
|
ENSP00000480279.1:p.Ala39=
|
|
NM_001282489.2:c.-140T>A
(USH1G)
|
NP_001269418.1:n.-140T>A
|
|
NM_173477.4:c.117T>A
(USH1G)
|
NP_775748.2:p.Ala39=
|
|
XM_011525479.2:c.-308A>T
(OTOP2)
|
XP_011523781.1:n.-308A>T
|
|
NM_173477.5:c.117T>A
(USH1G)
MANE Select
|
NP_775748.2:p.Ala39=
|
|
NM_001282489.3:c.-140T>A
(USH1G)
|
NP_001269418.1:n.-140T>A
|
|