ENST00000370060.7:c.3509A>T
MANE Select
|
ENSP00000359077.1:p.Asp1170Val
|
|
ENST00000361699.8:c.3509A>T
|
ENSP00000355380.4:p.Asp1170Val
|
|
ENST00000361981.7:c.3494A>T
|
ENSP00000354712.3:p.Asp1165Val
|
|
ENST00000370055.5:c.3494A>T
|
ENSP00000359072.1:p.Asp1165Val
|
|
ENST00000370058.7:c.209A>T
|
ENSP00000359075.3:p.Asp70Val
|
|
ENST00000370060.5:c.3509A>T
|
ENSP00000359077.1:p.Asp1170Val
|
|
ENST00000491983.1:n.472A>T
|
|
|
NM_000425.4:c.3509A>T
|
NP_000416.1:p.Asp1170Val
|
|
NM_001143963.2:c.3494A>T
|
NP_001137435.1:p.Asp1165Val
|
|
NM_001278116.1:c.3509A>T
|
NP_001265045.1:p.Asp1170Val
|
|
NM_024003.3:c.3509A>T
|
NP_076493.1:p.Asp1170Val
|
|
NM_000425.5:c.3509A>T
|
NP_000416.1:p.Asp1170Val
|
|
NM_001278116.2:c.3509A>T
MANE Select
|
NP_001265045.1:p.Asp1170Val
|
|