ENST00000371375.2:c.4315G>A
|
ENSP00000360426.1:p.Ala1439Thr
|
|
ENST00000685253.1:c.*1782G>A
|
ENSP00000509405.1:n.*1782G>A
|
|
ENST00000685889.1:n.1974G>A
|
|
|
ENST00000686807.1:n.658G>A
|
|
|
ENST00000686954.1:c.*523G>A
|
ENSP00000508416.1:n.*523G>A
|
|
ENST00000688810.1:c.4267G>A
|
ENSP00000509140.1:p.Ala1423Thr
|
|
ENST00000689233.1:n.9447G>A
|
|
|
ENST00000690340.1:n.2912G>A
|
|
|
ENST00000692286.1:c.5107G>A
|
ENSP00000509490.1:p.Ala1703Thr
|
|
ENST00000692396.1:c.5191G>A
|
ENSP00000508605.1:p.Ala1731Thr
|
|
ENST00000371380.8:c.5239G>A
MANE Select
|
ENSP00000360431.2:p.Ala1747Thr
|
|
ENST00000371385.8:c.4213G>A
|
ENSP00000360438.4:p.Ala1405Thr
|
|
ENST00000674738.1:c.3794G>A
|
|
|
ENST00000674827.1:c.3355G>A
|
ENSP00000502523.1:p.Ala1119Thr
|
|
ENST00000675218.1:c.4315G>A
|
ENSP00000501910.1:p.Ala1439Thr
|
|
ENST00000675487.1:c.*1172G>A
|
ENSP00000502340.1:n.*1172G>A
|
|
ENST00000675718.1:c.4508G>A
|
|
|
ENST00000676102.1:c.4084G>A
|
ENSP00000502811.1:p.Ala1362Thr
|
|
ENST00000260766.7:c.5239G>A
|
ENSP00000260766.3:p.Ala1747Thr
|
|
ENST00000371375.1:c.4315G>A
|
ENSP00000360426.1:p.Ala1439Thr
|
|
ENST00000371380.7:c.5239G>A
|
ENSP00000360431.2:p.Ala1747Thr
|
|
ENST00000371385.7:c.4315G>A
|
ENSP00000360438.3:p.Ala1439Thr
|
|
NM_001165979.2:c.4315G>A
|
NP_001159451.1:p.Ala1439Thr
|
|
NM_001288989.1:c.5191G>A
|
NP_001275918.1:p.Ala1731Thr
|
|
NM_016341.3:c.5239G>A
|
NP_057425.3:p.Ala1747Thr
|
|
XM_006717885.2:c.5281G>A
|
XP_006717948.1:p.Ala1761Thr
|
|
XM_006717886.2:c.5281G>A
|
XP_006717949.1:p.Ala1761Thr
|
|
XM_006717888.2:c.5278G>A
|
XP_006717951.1:p.Ala1760Thr
|
|
XM_006717889.2:c.5233G>A
|
XP_006717952.1:p.Ala1745Thr
|
|
XM_006717890.1:c.4357G>A
|
XP_006717953.1:p.Ala1453Thr
|
|
XM_011539849.1:c.5281G>A
|
XP_011538151.1:p.Ala1761Thr
|
|
XM_011539850.1:c.4126G>A
|
XP_011538152.1:p.Ala1376Thr
|
|
XM_006717885.4:c.5281G>A
|
XP_006717948.1:p.Ala1761Thr
|
|
XM_006717888.4:c.5278G>A
|
XP_006717951.1:p.Ala1760Thr
|
|
XM_006717889.4:c.5233G>A
|
XP_006717952.1:p.Ala1745Thr
|
|
XM_006717890.3:c.4357G>A
|
XP_006717953.1:p.Ala1453Thr
|
|
XM_011539849.3:c.5281G>A
|
XP_011538151.1:p.Ala1761Thr
|
|
XM_011539850.3:c.4126G>A
|
XP_011538152.1:p.Ala1376Thr
|
|
XM_017016310.2:c.5281G>A
|
XP_016871799.1:p.Ala1761Thr
|
|
XM_017016311.2:c.5281G>A
|
XP_016871800.1:p.Ala1761Thr
|
|
XM_017016312.2:c.4267G>A
|
XP_016871801.1:p.Ala1423Thr
|
|
NM_001288989.2:c.5191G>A
|
NP_001275918.1:p.Ala1731Thr
|
|
NM_016341.4:c.5239G>A
MANE Select
|
NP_057425.3:p.Ala1747Thr
|
|