ENST00000359595.8:c.467G>C
MANE Select
|
ENSP00000352606.4:p.Ser156Thr
|
|
ENST00000359595.7:c.467G>C
|
ENSP00000352606.3:p.Ser156Thr
|
|
ENST00000558770.5:c.467G>C
|
ENSP00000456458.1:p.Ser156Thr
|
|
ENST00000562281.1:c.467G>C
|
ENSP00000456985.1:p.Ser156Thr
|
|
ENST00000562889.5:c.653G>C
|
ENSP00000457180.1:p.Ser218Thr
|
|
ENST00000563808.1:n.569G>C
|
|
|
NM_001307952.1:c.653G>C
|
NP_001294881.1:p.Ser218Thr
|
|
NM_178232.2:c.467G>C
|
NP_839946.1:p.Ser156Thr
|
|
NM_178232.3:c.467G>C
|
NP_839946.1:p.Ser156Thr
|
|
XM_011521261.1:c.599G>C
|
XP_011519563.1:p.Ser200Thr
|
|
XR_243204.1:n.682G>C
|
|
|
XR_931756.1:n.788G>C
|
|
|
XM_017021934.2:c.653G>C
|
XP_016877423.1:p.Ser218Thr
|
|
XM_017021935.2:c.88G>C
|
XP_016877424.1:p.Ala30Pro
|
|
XM_017021936.2:c.88G>C
|
XP_016877425.1:p.Ala30Pro
|
|
XR_001751098.2:n.800G>C
|
|
|
XR_931756.3:n.801G>C
|
|
|
NM_001307952.2:c.653G>C
|
NP_001294881.1:p.Ser218Thr
|
|
NM_178232.4:c.467G>C
MANE Select
|
NP_839946.1:p.Ser156Thr
|
|