ENST00000380044.6:c.161T>C
MANE Select
|
ENSP00000369383.1:p.Met54Thr
|
|
ENST00000233545.6:c.161T>C
|
ENSP00000233545.2:p.Met54Thr
|
|
ENST00000357186.10:c.19-247T>C
|
ENSP00000349713.6:n.19-247T>C
|
|
ENST00000380044.5:c.161T>C
|
ENSP00000369383.1:p.Met54Thr
|
|
ENST00000402310.5:c.161T>C
|
ENSP00000383955.1:p.Met54Thr
|
|
ENST00000402722.5:c.126T>C
|
ENSP00000386000.1:p.His42=
|
|
ENST00000403262.6:c.161T>C
|
ENSP00000385671.1:p.Met54Thr
|
|
ENST00000405076.5:c.161T>C
|
ENSP00000385175.1:p.Met54Thr
|
|
ENST00000405983.5:c.206T>C
|
ENSP00000384586.1:p.Met69Thr
|
|
ENST00000415514.5:c.228-247T>C
|
ENSP00000388043.1:n.228-247T>C
|
|
ENST00000426513.6:c.126T>C
|
ENSP00000403824.2:p.His42=
|
|
ENST00000428910.5:c.83T>C
|
ENSP00000405235.1:p.Met28Thr
|
|
ENST00000430991.5:c.91T>C
|
|
|
ENST00000616446.1:n.138T>C
|
|
|
ENST00000616707.1:n.369T>C
|
|
|
ENST00000617583.4:n.187T>C
|
|
|
ENST00000621183.4:n.217T>C
|
|
|
ENST00000621470.4:n.177T>C
|
|
|
ENST00000622003.4:n.334T>C
|
|
|
NM_002437.4:c.161T>C
|
NP_002428.1:p.Met54Thr
|
|
XM_005264326.2:c.161T>C
|
XP_005264383.1:p.Met54Thr
|
|
XM_005264327.2:c.2T>C
|
XP_005264384.1:p.Met1Thr
|
|
XM_006712021.2:c.113T>C
|
XP_006712084.1:p.Met38Thr
|
|
XM_005264326.4:c.161T>C
|
XP_005264383.1:p.Met54Thr
|
|
XM_006712021.3:c.113T>C
|
XP_006712084.1:p.Met38Thr
|
|
XM_017004150.1:c.143T>C
|
XP_016859639.1:p.Met48Thr
|
|
XM_017004151.1:c.113T>C
|
XP_016859640.1:p.Met38Thr
|
|
XM_017004152.1:c.2T>C
|
XP_016859641.1:p.Met1Thr
|
|
XM_024452913.1:c.113T>C
|
XP_024308681.1:p.Met38Thr
|
|
NM_002437.5:c.161T>C
MANE Select
|
NP_002428.1:p.Met54Thr
|
|