ENST00000372163.5:c.393+310A>G
(RSPH9)
MANE Select
|
ENSP00000361236.4:n.393+310A>G
|
|
ENST00000372163.4:c.393+310A>G
(RSPH9)
|
ENSP00000361236.4:n.393+310A>G
|
|
ENST00000372165.8:c.393+310A>G
(RSPH9)
|
ENSP00000361238.4:n.393+310A>G
|
|
NM_001193341.1:c.393+310A>G
(RSPH9)
|
NP_001180270.1:n.393+310A>G
|
|
NM_152732.4:c.393+310A>G
(RSPH9)
|
NP_689945.2:n.393+310A>G
|
|
XM_005248901.2:c.393+310A>G
(RSPH9)
|
XP_005248958.1:n.393+310A>G
|
|
XM_006715014.1:c.228-4712A>G
(RSPH9)
|
XP_006715077.1:n.228-4712A>G
|
|
XM_011514356.1:c.393+310A>G
(RSPH9)
|
XP_011512658.1:n.393+310A>G
|
|
XR_926099.1:n.428+310A>G
(RSPH9)
|
|
|
XM_005248901.3:c.393+310A>G
(RSPH9)
|
XP_005248958.1:n.393+310A>G
|
|
XR_002956268.1:n.435+310A>G
(RSPH9)
|
|
|
XR_002956269.1:n.297-4712A>G
(RSPH9)
|
|
|
XR_926099.2:n.435+310A>G
(RSPH9)
|
|
|
NM_152732.5:c.393+310A>G
(RSPH9)
MANE Select
|
NP_689945.2:n.393+310A>G
|
|
NM_001193341.2:c.393+310A>G
(RSPH9)
|
NP_001180270.1:n.393+310A>G
|
|
NM_001318876.2:c.945+121579A>G
(POLR1C)
|
NP_001305805.1:n.945+121579A>G
|
|