|
ENST00000371375.2:c.4444G>A
|
ENSP00000360426.1:p.Ala1482Thr
|
|
|
ENST00000685253.1:c.*1911G>A
|
ENSP00000509405.1:n.*1911G>A
|
|
|
ENST00000685889.1:n.2103G>A
|
|
|
|
ENST00000686807.1:n.787G>A
|
|
|
|
ENST00000686954.1:c.*652G>A
|
ENSP00000508416.1:n.*652G>A
|
|
|
ENST00000688810.1:c.4396G>A
|
ENSP00000509140.1:p.Ala1466Thr
|
|
|
ENST00000689233.1:n.9576G>A
|
|
|
|
ENST00000690340.1:n.3041G>A
|
|
|
|
ENST00000692286.1:c.5236G>A
|
ENSP00000509490.1:p.Ala1746Thr
|
|
|
ENST00000692396.1:c.5320G>A
|
ENSP00000508605.1:p.Ala1774Thr
|
|
|
ENST00000371380.8:c.5368G>A
MANE Select
|
ENSP00000360431.2:p.Ala1790Thr
|
|
|
ENST00000371385.8:c.4342G>A
|
ENSP00000360438.4:p.Ala1448Thr
|
|
|
ENST00000674738.1:c.3923G>A
|
|
|
|
ENST00000674827.1:c.3484G>A
|
ENSP00000502523.1:p.Ala1162Thr
|
|
|
ENST00000675218.1:c.4444G>A
|
ENSP00000501910.1:p.Ala1482Thr
|
|
|
ENST00000675487.1:c.*1301G>A
|
ENSP00000502340.1:n.*1301G>A
|
|
|
ENST00000675718.1:c.4637G>A
|
|
|
|
ENST00000260766.7:c.5368G>A
|
ENSP00000260766.3:p.Ala1790Thr
|
|
|
ENST00000371375.1:c.4444G>A
|
ENSP00000360426.1:p.Ala1482Thr
|
|
|
ENST00000371380.7:c.5368G>A
|
ENSP00000360431.2:p.Ala1790Thr
|
|
|
ENST00000371385.7:c.4444G>A
|
ENSP00000360438.3:p.Ala1482Thr
|
|
|
NM_001165979.2:c.4444G>A
|
NP_001159451.1:p.Ala1482Thr
|
|
|
NM_001288989.1:c.5320G>A
|
NP_001275918.1:p.Ala1774Thr
|
|
|
NM_016341.3:c.5368G>A
|
NP_057425.3:p.Ala1790Thr
|
|
|
XM_006717885.2:c.5410G>A
|
XP_006717948.1:p.Ala1804Thr
|
|
|
XM_006717886.2:c.5410G>A
|
XP_006717949.1:p.Ala1804Thr
|
|
|
XM_006717888.2:c.5407G>A
|
XP_006717951.1:p.Ala1803Thr
|
|
|
XM_006717889.2:c.5362G>A
|
XP_006717952.1:p.Ala1788Thr
|
|
|
XM_006717890.1:c.4486G>A
|
XP_006717953.1:p.Ala1496Thr
|
|
|
XM_011539849.1:c.5410G>A
|
XP_011538151.1:p.Ala1804Thr
|
|
|
XM_011539850.1:c.4255G>A
|
XP_011538152.1:p.Ala1419Thr
|
|
|
XM_006717885.4:c.5410G>A
|
XP_006717948.1:p.Ala1804Thr
|
|
|
XM_006717888.4:c.5407G>A
|
XP_006717951.1:p.Ala1803Thr
|
|
|
XM_006717889.4:c.5362G>A
|
XP_006717952.1:p.Ala1788Thr
|
|
|
XM_006717890.3:c.4486G>A
|
XP_006717953.1:p.Ala1496Thr
|
|
|
XM_011539849.3:c.5410G>A
|
XP_011538151.1:p.Ala1804Thr
|
|
|
XM_011539850.3:c.4255G>A
|
XP_011538152.1:p.Ala1419Thr
|
|
|
XM_017016310.2:c.5410G>A
|
XP_016871799.1:p.Ala1804Thr
|
|
|
XM_017016311.2:c.5410G>A
|
XP_016871800.1:p.Ala1804Thr
|
|
|
XM_017016312.2:c.4396G>A
|
XP_016871801.1:p.Ala1466Thr
|
|
|
NM_001288989.2:c.5320G>A
|
NP_001275918.1:p.Ala1774Thr
|
|
|
NM_016341.4:c.5368G>A
MANE Select
|
NP_057425.3:p.Ala1790Thr
|
|
