ENST00000697713.1:c.*3A>G
(RAG1)
|
ENSP00000513411.1:n.*3A>G
|
|
ENST00000697714.1:c.*3A>G
(RAG1)
|
ENSP00000513412.1:n.*3A>G
|
|
ENST00000697715.1:c.*3A>G
(RAG1)
|
ENSP00000513413.1:n.*3A>G
|
|
ENST00000299440.6:c.*3A>G
(RAG1)
MANE Select
|
ENSP00000299440.5:n.*3A>G
|
|
ENST00000299440.5:c.*3A>G
(RAG1)
|
ENSP00000299440.5:n.*3A>G
|
|
ENST00000524423.1:n.132-468T>C
(RAG2)
|
|
|
ENST00000534663.1:c.2789+346A>G
(RAG1)
|
ENSP00000434610.1:n.2789+346A>G
|
|
NM_000448.2:c.*3A>G , LRG_98t1:c.*3A>G
(RAG1)
|
NP_000439.1:n.*3A>G
|
|
XM_005253041.3:c.*3A>G
(RAG1)
|
XP_005253098.1:n.*3A>G
|
|
XM_011520250.1:c.*3A>G
(RAG1)
|
XP_011518552.1:n.*3A>G
|
|
XM_011520251.1:c.*3A>G
(RAG1)
|
XP_011518553.1:n.*3A>G
|
|
XM_005253041.4:c.*3A>G
(RAG1)
|
XP_005253098.1:n.*3A>G
|
|
XM_011520250.2:c.*3A>G
(RAG1)
|
XP_011518552.1:n.*3A>G
|
|
NM_000448.3:c.*3A>G
(RAG1)
MANE Select
|
NP_000439.2:n.*3A>G
|
|
NM_001377277.1:c.*3A>G
(RAG1)
|
NP_001364206.1:n.*3A>G
|
|
NM_001377278.1:c.*3A>G
(RAG1)
|
NP_001364207.1:n.*3A>G
|
|
NM_001377279.1:c.*3A>G
(RAG1)
|
NP_001364208.1:n.*3A>G
|
|
NM_001377280.1:c.*3A>G
(RAG1)
|
NP_001364209.1:n.*3A>G
|
|