ENST00000355773.6:c.1318G>C
MANE Select
|
ENSP00000348019.5:p.Gly440Arg
|
|
ENST00000355773.5:c.1318G>C
|
ENSP00000348019.5:p.Gly440Arg
|
|
NM_012434.4:c.1318G>C
|
NP_036566.1:p.Gly440Arg
|
|
XM_005248710.2:c.1267G>C
|
XP_005248767.1:p.Gly423Arg
|
|
XM_005248711.1:c.1120G>C
|
XP_005248768.1:p.Gly374Arg
|
|
XM_011535750.1:c.1170G>C
|
XP_011534052.1:p.Leu390Phe
|
|
NM_012434.5:c.1318G>C
MANE Select
|
NP_036566.1:p.Gly440Arg
|
|
NM_001382629.1:c.1087G>C
|
NP_001369558.1:p.Gly363Arg
|
|
NM_001382630.1:c.1260-5169G>C
|
NP_001369559.1:n.1260-5169G>C
|
|
NM_001382631.1:c.1339G>C
|
NP_001369560.1:p.Gly447Arg
|
|
NM_001382632.1:c.1231G>C
|
NP_001369561.1:p.Gly411Arg
|
|
NM_001382633.1:c.1318G>C
|
NP_001369562.1:p.Gly440Arg
|
|
NM_001382634.1:c.1159G>C
|
NP_001369563.1:p.Gly387Arg
|
|
NM_001382635.1:c.1315G>C
|
NP_001369564.1:p.Gly439Arg
|
|
NM_001382636.1:c.1000G>C
|
NP_001369565.1:p.Gly334Arg
|
|