ENST00000371375.2:c.4285T>A
|
ENSP00000360426.1:p.Ser1429Thr
|
|
ENST00000685253.1:c.*1752T>A
|
ENSP00000509405.1:n.*1752T>A
|
|
ENST00000685889.1:n.1944T>A
|
|
|
ENST00000686807.1:n.628T>A
|
|
|
ENST00000686954.1:c.*493T>A
|
ENSP00000508416.1:n.*493T>A
|
|
ENST00000688810.1:c.4237T>A
|
ENSP00000509140.1:p.Ser1413Thr
|
|
ENST00000689233.1:n.9417T>A
|
|
|
ENST00000690340.1:n.2882T>A
|
|
|
ENST00000692286.1:c.5077T>A
|
ENSP00000509490.1:p.Ser1693Thr
|
|
ENST00000692396.1:c.5161T>A
|
ENSP00000508605.1:p.Ser1721Thr
|
|
ENST00000371380.8:c.5209T>A
MANE Select
|
ENSP00000360431.2:p.Ser1737Thr
|
|
ENST00000371385.8:c.4183T>A
|
ENSP00000360438.4:p.Ser1395Thr
|
|
ENST00000674738.1:c.3764T>A
|
|
|
ENST00000674827.1:c.3325T>A
|
ENSP00000502523.1:p.Ser1109Thr
|
|
ENST00000675218.1:c.4285T>A
|
ENSP00000501910.1:p.Ser1429Thr
|
|
ENST00000675487.1:c.*1142T>A
|
ENSP00000502340.1:n.*1142T>A
|
|
ENST00000675718.1:c.4478T>A
|
|
|
ENST00000676102.1:c.4054T>A
|
ENSP00000502811.1:p.Ser1352Thr
|
|
ENST00000260766.7:c.5209T>A
|
ENSP00000260766.3:p.Ser1737Thr
|
|
ENST00000371375.1:c.4285T>A
|
ENSP00000360426.1:p.Ser1429Thr
|
|
ENST00000371380.7:c.5209T>A
|
ENSP00000360431.2:p.Ser1737Thr
|
|
ENST00000371385.7:c.4285T>A
|
ENSP00000360438.3:p.Ser1429Thr
|
|
NM_001165979.2:c.4285T>A
|
NP_001159451.1:p.Ser1429Thr
|
|
NM_001288989.1:c.5161T>A
|
NP_001275918.1:p.Ser1721Thr
|
|
NM_016341.3:c.5209T>A
|
NP_057425.3:p.Ser1737Thr
|
|
XM_006717885.2:c.5251T>A
|
XP_006717948.1:p.Ser1751Thr
|
|
XM_006717886.2:c.5251T>A
|
XP_006717949.1:p.Ser1751Thr
|
|
XM_006717888.2:c.5248T>A
|
XP_006717951.1:p.Ser1750Thr
|
|
XM_006717889.2:c.5203T>A
|
XP_006717952.1:p.Ser1735Thr
|
|
XM_006717890.1:c.4327T>A
|
XP_006717953.1:p.Ser1443Thr
|
|
XM_011539849.1:c.5251T>A
|
XP_011538151.1:p.Ser1751Thr
|
|
XM_011539850.1:c.4096T>A
|
XP_011538152.1:p.Ser1366Thr
|
|
XM_006717885.4:c.5251T>A
|
XP_006717948.1:p.Ser1751Thr
|
|
XM_006717888.4:c.5248T>A
|
XP_006717951.1:p.Ser1750Thr
|
|
XM_006717889.4:c.5203T>A
|
XP_006717952.1:p.Ser1735Thr
|
|
XM_006717890.3:c.4327T>A
|
XP_006717953.1:p.Ser1443Thr
|
|
XM_011539849.3:c.5251T>A
|
XP_011538151.1:p.Ser1751Thr
|
|
XM_011539850.3:c.4096T>A
|
XP_011538152.1:p.Ser1366Thr
|
|
XM_017016310.2:c.5251T>A
|
XP_016871799.1:p.Ser1751Thr
|
|
XM_017016311.2:c.5251T>A
|
XP_016871800.1:p.Ser1751Thr
|
|
XM_017016312.2:c.4237T>A
|
XP_016871801.1:p.Ser1413Thr
|
|
NM_001288989.2:c.5161T>A
|
NP_001275918.1:p.Ser1721Thr
|
|
NM_016341.4:c.5209T>A
MANE Select
|
NP_057425.3:p.Ser1737Thr
|
|