ENST00000359595.8:c.156G>C
MANE Select
|
ENSP00000352606.4:p.Glu52Asp
|
|
ENST00000359595.7:c.156G>C
|
ENSP00000352606.3:p.Glu52Asp
|
|
ENST00000558770.5:c.156G>C
|
ENSP00000456458.1:p.Glu52Asp
|
|
ENST00000562281.1:c.156G>C
|
ENSP00000456985.1:p.Glu52Asp
|
|
ENST00000562889.5:c.342G>C
|
ENSP00000457180.1:p.Glu114Asp
|
|
ENST00000563808.1:n.258G>C
|
|
|
NM_001307952.1:c.342G>C
|
NP_001294881.1:p.Glu114Asp
|
|
NM_178232.2:c.156G>C
|
NP_839946.1:p.Glu52Asp
|
|
NM_178232.3:c.156G>C
|
NP_839946.1:p.Glu52Asp
|
|
XM_011521261.1:c.288G>C
|
XP_011519563.1:p.Glu96Asp
|
|
XR_243204.1:n.371G>C
|
|
|
XR_931756.1:n.477G>C
|
|
|
XM_017021934.2:c.342G>C
|
XP_016877423.1:p.Glu114Asp
|
|
XM_017021935.2:c.-224G>C
|
XP_016877424.1:n.-224G>C
|
|
XM_017021936.2:c.-224G>C
|
XP_016877425.1:n.-224G>C
|
|
XR_001751098.2:n.489G>C
|
|
|
XR_931756.3:n.490G>C
|
|
|
NM_001307952.2:c.342G>C
|
NP_001294881.1:p.Glu114Asp
|
|
NM_178232.4:c.156G>C
MANE Select
|
NP_839946.1:p.Glu52Asp
|
|