|
NM_000969.5:c.385G>T
(RPL5)
MANE Select
|
NP_000960.2:p.Glu129Ter
|
|
ENST00000370321.8:c.385G>T
(RPL5)
MANE Select
|
ENSP00000359345.2:p.Glu129Ter
|
|
NM_000969.3:c.385G>T
(RPL5)
|
NP_000960.2:p.Glu129Ter
|
|
NM_001252273.1:c.475-3216C>A
(DIPK1A)
|
NP_001239202.1:n.475-3216C>A
|
|
NM_001252273.2:c.475-3216C>A
(DIPK1A)
|
NP_001239202.1:n.475-3216C>A
|
|
NR_146333.1:n.444G>T
(RPL5)
|
|
|
ENST00000315741.5:c.235G>T
(RPL5)
|
ENSP00000359338.2:p.Glu79Ter
|
|
ENST00000370321.7:c.385G>T
(RPL5)
|
ENSP00000359345.2:p.Glu129Ter
|
|
ENST00000461952.1:n.1095G>T
(RPL5)
|
|
|
ENST00000470843.5:c.*347G>T
(RPL5)
|
ENSP00000473675.1:n.*347G>T
|
|
ENST00000615519.4:c.475-3216C>A
(DIPK1A)
|
ENSP00000483279.1:n.475-3216C>A
|
|
ENST00000645119.1:c.324+1337G>T
(RPL5)
|
ENSP00000493811.1:n.324+1337G>T
|
|
ENST00000645300.1:c.235G>T
(RPL5)
|
ENSP00000495589.1:p.Glu79Ter
|
|
ENST00000645908.1:n.119G>T
(RPL5)
|
|