ENST00000359595.8:c.457G=
MANE Select
|
ENSP00000352606.4:p.Glu153=
|
|
ENST00000359595.7:c.457G=
|
ENSP00000352606.3:p.Glu153=
|
|
ENST00000558770.5:c.457G=
|
ENSP00000456458.1:p.Glu153=
|
|
ENST00000562281.1:c.457G=
|
ENSP00000456985.1:p.Glu153=
|
|
ENST00000562889.5:c.643G=
|
ENSP00000457180.1:p.Glu215=
|
|
ENST00000563808.1:n.559G=
|
|
|
NM_001307952.1:c.643G=
|
NP_001294881.1:p.Glu215=
|
|
NM_178232.2:c.457G=
|
NP_839946.1:p.Glu153=
|
|
NM_178232.3:c.457G=
|
NP_839946.1:p.Glu153=
|
|
XM_011521261.1:c.589G=
|
XP_011519563.1:p.Glu197=
|
|
XR_243204.1:n.672G=
|
|
|
XR_931756.1:n.778G=
|
|
|
XM_017021934.2:c.643G=
|
XP_016877423.1:p.Glu215=
|
|
XM_017021935.2:c.78G=
|
XP_016877424.1:p.Trp26=
|
|
XM_017021936.2:c.78G=
|
XP_016877425.1:p.Trp26=
|
|
XR_001751098.2:n.790G=
|
|
|
XR_931756.3:n.791G=
|
|
|
NM_001307952.2:c.643G=
|
NP_001294881.1:p.Glu215=
|
|
NM_178232.4:c.457G=
MANE Select
|
NP_839946.1:p.Glu153=
|
|