ENST00000312251.8:c.837G>T
MANE Select
|
ENSP00000310998.3:p.Val279=
|
|
ENST00000649828.1:c.837G>T
|
ENSP00000498032.1:p.Val279=
|
|
ENST00000312251.7:c.837G>T
|
ENSP00000310998.3:p.Val279=
|
|
ENST00000381955.7:c.837G>T
|
ENSP00000371381.3:p.Val279=
|
|
ENST00000562037.1:c.598G>T
|
ENSP00000464994.1:n.598G>T
|
|
ENST00000562346.2:c.505-778G>T
|
|
|
ENST00000562746.5:c.837G>T
|
ENSP00000455900.1:p.Val279=
|
|
ENST00000563578.5:c.655G>T
|
|
|
ENST00000564397.5:n.1196G>T
|
|
|
ENST00000565876.5:c.480+1422G>T
|
|
|
ENST00000567739.5:n.156G>T
|
|
|
ENST00000568202.5:n.700G>T
|
|
|
ENST00000569296.5:c.381G>T
|
ENSP00000465949.1:p.Val127=
|
|
NM_016256.3:c.837G>T
|
NP_057340.2:p.Val279=
|
|
XM_011522517.1:c.837G>T
|
XP_011520819.1:p.Val279=
|
|
XM_011522518.1:c.837G>T
|
XP_011520820.1:p.Val279=
|
|
XM_011522519.1:c.837G>T
|
XP_011520821.1:p.Val279=
|
|
XR_243285.1:n.864G>T
|
|
|
XM_011522517.3:c.837G>T
|
XP_011520819.1:p.Val279=
|
|
XR_001751908.2:n.863G>T
|
|
|
XR_001751909.2:n.863G>T
|
|
|
XR_001751910.2:n.863G>T
|
|
|
XR_001751911.2:n.863G>T
|
|
|
XR_001751912.2:n.863G>T
|
|
|
NM_016256.4:c.837G>T
MANE Select
|
NP_057340.2:p.Val279=
|
|