ENST00000355773.6:c.1225G>C
MANE Select
|
ENSP00000348019.5:p.Gly409Arg
|
|
ENST00000355773.5:c.1225G>C
|
ENSP00000348019.5:p.Gly409Arg
|
|
NM_012434.4:c.1225G>C
|
NP_036566.1:p.Gly409Arg
|
|
XM_005248710.2:c.1174G>C
|
XP_005248767.1:p.Gly392Arg
|
|
XM_005248711.1:c.1027G>C
|
XP_005248768.1:p.Gly343Arg
|
|
XM_011535750.1:c.1111+4881G>C
|
XP_011534052.1:n.1111+4881G>C
|
|
NM_012434.5:c.1225G>C
MANE Select
|
NP_036566.1:p.Gly409Arg
|
|
NM_001382629.1:c.994G>C
|
NP_001369558.1:p.Gly332Arg
|
|
NM_001382630.1:c.1225G>C
|
NP_001369559.1:p.Gly409Arg
|
|
NM_001382631.1:c.1246G>C
|
NP_001369560.1:p.Gly416Arg
|
|
NM_001382632.1:c.1138G>C
|
NP_001369561.1:p.Gly380Arg
|
|
NM_001382633.1:c.1225G>C
|
NP_001369562.1:p.Gly409Arg
|
|
NM_001382634.1:c.1066G>C
|
NP_001369563.1:p.Gly356Arg
|
|
NM_001382635.1:c.1222G>C
|
NP_001369564.1:p.Gly408Arg
|
|
NM_001382636.1:c.907G>C
|
NP_001369565.1:p.Gly303Arg
|
|