ENST00000646375.2:c.*44G>T
(AVPR2)
MANE Select
|
ENSP00000496396.1:n.*44G>T
|
|
ENST00000434679.6:c.*526G>T
(AVPR2)
|
ENSP00000393397.1:n.*526G>T
|
|
ENST00000642393.1:c.97+2298C>A
|
|
|
ENST00000646191.1:c.97+2298C>A
|
|
|
ENST00000646375.1:c.*44G>T
(AVPR2)
|
ENSP00000496396.1:n.*44G>T
|
|
ENST00000337474.5:c.*44G>T
(AVPR2)
|
ENSP00000338072.5:n.*44G>T
|
|
ENST00000358927.6:c.*44G>T
(AVPR2)
|
ENSP00000351805.2:n.*44G>T
|
|
ENST00000370049.1:c.*336G>T
(AVPR2)
|
ENSP00000359066.1:n.*336G>T
|
|
ENST00000430697.1:c.1072G>T
(AVPR2)
|
ENSP00000393513.1:p.Ala358Ser
|
|
ENST00000434679.5:c.*526G>T
(AVPR2)
|
ENSP00000393397.1:n.*526G>T
|
|
ENST00000464967.5:n.154+2298C>A
(L1CAM)
|
|
|
NM_000054.4:c.*44G>T
(AVPR2)
|
NP_000045.1:n.*44G>T
|
|
NM_001146151.1:c.*336G>T
(AVPR2)
|
NP_001139623.1:n.*336G>T
|
|
NR_027419.1:n.1207G>T
(AVPR2)
|
|
|
XM_006724828.2:c.*44G>T
(AVPR2)
|
XP_006724891.1:n.*44G>T
|
|
NM_000054.5:c.*44G>T
(AVPR2)
|
NP_000045.1:n.*44G>T
|
|
NM_001146151.2:c.*336G>T
(AVPR2)
|
NP_001139623.1:n.*336G>T
|
|
XM_006724828.3:c.*44G>T
(AVPR2)
|
XP_006724891.1:n.*44G>T
|
|
NM_000054.6:c.*44G>T
(AVPR2)
|
NP_000045.1:n.*44G>T
|
|
NM_001146151.3:c.*336G>T
(AVPR2)
|
NP_001139623.1:n.*336G>T
|
|
NR_027419.2:n.1113G>T
(AVPR2)
|
|
|
NM_000054.7:c.*44G>T
(AVPR2)
MANE Select
|
NP_000045.1:n.*44G>T
|
|