|
ENST00000697713.1:c.2334G>T
(RAG1)
|
ENSP00000513411.1:p.Arg778=
|
|
|
ENST00000697714.1:c.2334G>T
(RAG1)
|
ENSP00000513412.1:p.Arg778=
|
|
|
ENST00000697715.1:c.2334G>T
(RAG1)
|
ENSP00000513413.1:p.Arg778=
|
|
|
ENST00000299440.6:c.2334G>T
(RAG1)
MANE Select
|
ENSP00000299440.5:p.Arg778=
|
|
|
ENST00000299440.5:c.2334G>T
(RAG1)
|
ENSP00000299440.5:p.Arg778=
|
|
|
ENST00000524423.1:n.465C>A
(RAG2)
|
|
|
|
ENST00000534663.1:c.2334G>T
(RAG1)
|
ENSP00000434610.1:p.Arg778=
|
|
|
NM_000448.2:c.2334G>T , LRG_98t1:c.2334G>T
(RAG1)
|
NP_000439.1:p.Arg778=
|
|
|
XM_005253041.3:c.2334G>T
(RAG1)
|
XP_005253098.1:p.Arg778=
|
|
|
XM_011520250.1:c.2334G>T
(RAG1)
|
XP_011518552.1:p.Arg778=
|
|
|
XM_011520251.1:c.2334G>T
(RAG1)
|
XP_011518553.1:p.Arg778=
|
|
|
XM_005253041.4:c.2334G>T
(RAG1)
|
XP_005253098.1:p.Arg778=
|
|
|
XM_011520250.2:c.2334G>T
(RAG1)
|
XP_011518552.1:p.Arg778=
|
|
|
NM_000448.3:c.2334G>T
(RAG1)
MANE Select
|
NP_000439.2:p.Arg778=
|
|
|
NM_001377277.1:c.2334G>T
(RAG1)
|
NP_001364206.1:p.Arg778=
|
|
|
NM_001377278.1:c.2334G>T
(RAG1)
|
NP_001364207.1:p.Arg778=
|
|
|
NM_001377279.1:c.2334G>T
(RAG1)
|
NP_001364208.1:p.Arg778=
|
|
|
NM_001377280.1:c.2334G>T
(RAG1)
|
NP_001364209.1:p.Arg778=
|
|
