ENST00000551171.6:c.693C>A
(RDH12)
MANE Select
|
ENSP00000449079.1:p.Gly231=
|
|
ENST00000267502.3:c.693C>A
(RDH12)
|
ENSP00000267502.3:p.Gly231=
|
|
ENST00000394455.6:n.3274G>T
(ZFYVE26)
|
|
|
ENST00000551171.5:c.693C>A
(RDH12)
|
ENSP00000449079.1:p.Gly231=
|
|
ENST00000552873.1:n.62C>A
(RDH12)
|
|
|
NM_152443.2:c.693C>A
(RDH12)
|
NP_689656.2:p.Gly231=
|
|
XM_017020925.2:c.1313-5970C>A
(GPHN)
|
XP_016876414.1:n.1313-5970C>A
|
|
XM_017021125.1:c.*517G>T
(ZFYVE26)
|
XP_016876614.1:n.*517G>T
|
|
NM_152443.3:c.693C>A
(RDH12)
MANE Select
|
NP_689656.2:p.Gly231=
|
|