ENST00000335304.6:c.*76G>A
(HTR3E)
|
ENSP00000335511.2:n.*76G>A
|
|
ENST00000415389.6:c.*76G>A
(HTR3E)
MANE Select
|
ENSP00000401444.2:n.*76G>A
|
|
NM_001256613.1:c.*76G>A
(HTR3E)
|
NP_001243542.1:n.*76G>A
|
|
NM_001256614.1:c.*76G>A
(HTR3E)
|
NP_001243543.1:n.*76G>A
|
|
NM_182589.2:c.*76G>A
(HTR3E)
|
NP_872395.2:n.*76G>A
|
|
NM_198313.2:c.*76G>A
(HTR3E)
|
NP_938055.1:n.*76G>A
|
|
NM_198314.2:c.*76G>A
(HTR3E)
|
NP_938056.1:n.*76G>A
|
|
XR_002959683.1:n.670+27767C>T
(EIF2B5-DT)
|
|
|
NM_001256613.2:c.*76G>A
(HTR3E)
MANE Select
|
NP_001243542.1:n.*76G>A
|
|
NM_198313.3:c.*76G>A
(HTR3E)
|
NP_938055.1:n.*76G>A
|
|