ENST00000542664.4:c.614-18682C=
(HTR2A)
MANE Select
|
ENSP00000437737.1:n.614-18682C=
|
|
ENST00000543956.5:c.125-18682C=
(HTR2A)
|
ENSP00000441861.2:n.125-18682C=
|
|
ENST00000378688.8:c.614-18682C=
(HTR2A)
|
ENSP00000367959.3:n.614-18682C=
|
|
ENST00000542664.3:c.614-18682C=
(HTR2A)
|
ENSP00000437737.1:n.614-18682C=
|
|
ENST00000543956.4:c.362-18682C=
(HTR2A)
|
ENSP00000441861.1:n.362-18682C=
|
|
NM_000621.4:c.614-18682C=
(HTR2A)
|
NP_000612.1:n.614-18682C=
|
|
NM_001165947.2:c.362-18682C=
(HTR2A)
|
NP_001159419.1:n.362-18682C=
|
|
NR_046612.1:n.231+239G=
(HTR2A-AS1)
|
|
|
NR_103752.1:n.88-1769G=
(HTR2A-AS1)
|
|
|
NM_000621.5:c.614-18682C=
(HTR2A)
MANE Select
|
NP_000612.1:n.614-18682C=
|
|
NM_001165947.5:c.125-18682C=
(HTR2A)
|
NP_001159419.2:n.125-18682C=
|
|
NM_001378924.1:c.614-18682C=
(HTR2A)
|
NP_001365853.1:n.614-18682C=
|
|