ENST00000646375.2:c.*111G>C
(AVPR2)
MANE Select
|
ENSP00000496396.1:n.*111G>C
|
|
ENST00000434679.6:c.*593G>C
(AVPR2)
|
ENSP00000393397.1:n.*593G>C
|
|
ENST00000642393.1:c.97+2231C>G
|
|
|
ENST00000646191.1:c.97+2231C>G
|
|
|
ENST00000646375.1:c.*111G>C
(AVPR2)
|
ENSP00000496396.1:n.*111G>C
|
|
ENST00000337474.5:c.*111G>C
(AVPR2)
|
ENSP00000338072.5:n.*111G>C
|
|
ENST00000358927.6:c.*111G>C
(AVPR2)
|
ENSP00000351805.2:n.*111G>C
|
|
ENST00000434679.5:c.*593G>C
(AVPR2)
|
ENSP00000393397.1:n.*593G>C
|
|
ENST00000464967.5:n.154+2231C>G
(L1CAM)
|
|
|
NM_000054.4:c.*111G>C
(AVPR2)
|
NP_000045.1:n.*111G>C
|
|
NM_001146151.1:c.*403G>C
(AVPR2)
|
NP_001139623.1:n.*403G>C
|
|
NR_027419.1:n.1274G>C
(AVPR2)
|
|
|
XM_006724828.2:c.*111G>C
(AVPR2)
|
XP_006724891.1:n.*111G>C
|
|
NM_000054.5:c.*111G>C
(AVPR2)
|
NP_000045.1:n.*111G>C
|
|
NM_001146151.2:c.*403G>C
(AVPR2)
|
NP_001139623.1:n.*403G>C
|
|
XM_006724828.3:c.*111G>C
(AVPR2)
|
XP_006724891.1:n.*111G>C
|
|
NM_000054.6:c.*111G>C
(AVPR2)
|
NP_000045.1:n.*111G>C
|
|
NM_001146151.3:c.*403G>C
(AVPR2)
|
NP_001139623.1:n.*403G>C
|
|
NR_027419.2:n.1180G>C
(AVPR2)
|
|
|
NM_000054.7:c.*111G>C
(AVPR2)
MANE Select
|
NP_000045.1:n.*111G>C
|
|