ENST00000366779.6:c.1138A>G
|
ENSP00000355741.2:p.Thr380Ala
|
|
ENST00000366782.6:c.1138A>G
|
ENSP00000355746.2:p.Thr380Ala
|
|
ENST00000366783.8:c.1138A>G
MANE Select
|
ENSP00000355747.3:p.Thr380Ala
|
|
ENST00000471728.2:n.1776A>G
|
|
|
ENST00000524196.6:c.1138A>G
|
ENSP00000429036.2:p.Thr380Ala
|
|
ENST00000626989.3:c.1138A>G
|
ENSP00000486498.2:p.Thr380Ala
|
|
ENST00000676467.1:c.*965A>G
|
ENSP00000504294.1:n.*965A>G
|
|
ENST00000676747.1:c.1135A>G
|
ENSP00000503244.1:p.Thr379Ala
|
|
ENST00000676884.1:c.1138A>G
|
ENSP00000503200.1:p.Thr380Ala
|
|
ENST00000676888.1:c.*479A>G
|
ENSP00000504483.1:n.*479A>G
|
|
ENST00000676907.1:c.*717A>G
|
ENSP00000504410.1:n.*717A>G
|
|
ENST00000676945.1:c.1138A>G
|
ENSP00000504433.1:p.Thr380Ala
|
|
ENST00000677065.1:n.1699A>G
|
|
|
ENST00000677414.1:c.1138A>G
|
ENSP00000503116.1:p.Thr380Ala
|
|
ENST00000677529.1:n.2868A>G
|
|
|
ENST00000677596.1:c.*1360A>G
|
ENSP00000503618.1:n.*1360A>G
|
|
ENST00000677599.1:c.1138A>G
|
ENSP00000503673.1:p.Thr380Ala
|
|
ENST00000677748.1:n.3393A>G
|
|
|
ENST00000677880.1:c.703A>G
|
ENSP00000503121.1:p.Thr235Ala
|
|
ENST00000678021.1:c.*761A>G
|
ENSP00000504674.1:n.*761A>G
|
|
ENST00000678233.1:c.1138A>G
|
ENSP00000504728.1:p.Thr380Ala
|
|
ENST00000678320.1:c.1039A>G
|
ENSP00000503680.1:p.Thr347Ala
|
|
ENST00000678655.1:c.1039A>G
|
ENSP00000504230.1:p.Thr347Ala
|
|
ENST00000678706.1:c.*515A>G
|
ENSP00000503659.1:n.*515A>G
|
|
ENST00000678776.1:c.*1275A>G
|
ENSP00000504624.1:n.*1275A>G
|
|
ENST00000678784.1:c.1072+2228A>G
|
ENSP00000504652.1:n.1072+2228A>G
|
|
ENST00000678820.1:c.1036A>G
|
ENSP00000504138.1:p.Thr346Ala
|
|
ENST00000678835.1:c.*756+2228A>G
|
ENSP00000504343.1:n.*756+2228A>G
|
|
ENST00000679088.1:c.1138A>G
|
ENSP00000504727.1:p.Thr380Ala
|
|
ENST00000679098.1:c.1138A>G
|
ENSP00000504303.1:p.Thr380Ala
|
|
ENST00000366782.5:c.1237A>G
|
ENSP00000355746.1:p.Thr413Ala
|
|
ENST00000366783.7:c.1138A>G
|
ENSP00000355747.3:p.Thr380Ala
|
|
ENST00000422240.6:c.1135A>G
|
ENSP00000403737.2:p.Thr379Ala
|
|
ENST00000471728.1:n.396A>G
|
|
|
ENST00000472139.2:c.706A>G
|
ENSP00000427806.1:p.Thr236Ala
|
|
ENST00000626989.2:c.1237A>G
|
ENSP00000486498.1:p.Thr413Ala
|
|
NM_000447.2:c.1138A>G
|
NP_000438.2:p.Thr380Ala
|
|
NM_012486.2:c.1135A>G
|
NP_036618.2:p.Thr379Ala
|
|
XM_005273199.2:c.1138A>G
|
XP_005273256.1:p.Thr380Ala
|
|
XM_011544236.1:c.706A>G
|
XP_011542538.1:p.Thr236Ala
|
|
XR_949149.1:n.1872A>G
|
|
|
XM_005273199.4:c.1138A>G
|
XP_005273256.1:p.Thr380Ala
|
|
XM_017001835.1:c.1138A>G
|
XP_016857324.1:p.Thr380Ala
|
|
XM_017001836.1:c.1135A>G
|
XP_016857325.1:p.Thr379Ala
|
|
XR_001737316.2:n.1477+2228A>G
|
|
|
XR_001737317.2:n.1477+2228A>G
|
|
|
XR_001737318.2:n.1853A>G
|
|
|
XR_001737319.1:n.2196A>G
|
|
|
XR_001737320.1:n.2193A>G
|
|
|
XR_001737321.1:n.1688A>G
|
|
|
XR_949149.2:n.1850A>G
|
|
|
XR_949150.3:n.2069A>G
|
|
|
NM_000447.3:c.1138A>G
MANE Select
|
NP_000438.2:p.Thr380Ala
|
|
NM_012486.3:c.1135A>G
|
NP_036618.2:p.Thr379Ala
|
|