ENST00000646375.2:c.*19G>T
(AVPR2)
MANE Select
|
ENSP00000496396.1:n.*19G>T
|
|
ENST00000434679.6:c.*501G>T
(AVPR2)
|
ENSP00000393397.1:n.*501G>T
|
|
ENST00000642393.1:c.97+2323C>A
|
|
|
ENST00000646191.1:c.97+2323C>A
|
|
|
ENST00000646375.1:c.*19G>T
(AVPR2)
|
ENSP00000496396.1:n.*19G>T
|
|
ENST00000337474.5:c.*19G>T
(AVPR2)
|
ENSP00000338072.5:n.*19G>T
|
|
ENST00000358927.6:c.*19G>T
(AVPR2)
|
ENSP00000351805.2:n.*19G>T
|
|
ENST00000370049.1:c.*311G>T
(AVPR2)
|
ENSP00000359066.1:n.*311G>T
|
|
ENST00000430697.1:c.1047G>T
(AVPR2)
|
ENSP00000393513.1:p.Leu349Phe
|
|
ENST00000434679.5:c.*501G>T
(AVPR2)
|
ENSP00000393397.1:n.*501G>T
|
|
ENST00000464967.5:n.154+2323C>A
(L1CAM)
|
|
|
NM_000054.4:c.*19G>T
(AVPR2)
|
NP_000045.1:n.*19G>T
|
|
NM_001146151.1:c.*311G>T
(AVPR2)
|
NP_001139623.1:n.*311G>T
|
|
NR_027419.1:n.1182G>T
(AVPR2)
|
|
|
XM_006724828.2:c.*19G>T
(AVPR2)
|
XP_006724891.1:n.*19G>T
|
|
NM_000054.5:c.*19G>T
(AVPR2)
|
NP_000045.1:n.*19G>T
|
|
NM_001146151.2:c.*311G>T
(AVPR2)
|
NP_001139623.1:n.*311G>T
|
|
XM_006724828.3:c.*19G>T
(AVPR2)
|
XP_006724891.1:n.*19G>T
|
|
NM_000054.6:c.*19G>T
(AVPR2)
|
NP_000045.1:n.*19G>T
|
|
NM_001146151.3:c.*311G>T
(AVPR2)
|
NP_001139623.1:n.*311G>T
|
|
NR_027419.2:n.1088G>T
(AVPR2)
|
|
|
NM_000054.7:c.*19G>T
(AVPR2)
MANE Select
|
NP_000045.1:n.*19G>T
|
|