|
ENST00000256578.8:c.1417T>G
|
ENSP00000256578.4:p.Ser473Ala
|
|
|
ENST00000358729.9:c.1417T>G
|
ENSP00000351573.5:p.Ser473Ala
|
|
|
ENST00000369840.7:c.1417T>G
|
ENSP00000358855.3:p.Ser473Ala
|
|
|
ENST00000474459.6:n.2036T>G
|
|
|
|
ENST00000476688.3:c.1099T>G
|
ENSP00000437025.2:p.Ser367Ala
|
|
|
ENST00000486282.7:n.2373T>G
|
|
|
|
ENST00000524975.2:n.1898T>G
|
|
|
|
ENST00000525415.2:n.1933T>G
|
|
|
|
ENST00000526301.6:n.1480T>G
|
|
|
|
ENST00000527846.7:n.1272T>G
|
|
|
|
ENST00000528667.7:c.1417T>G
MANE Select
|
ENSP00000436541.2:p.Ser473Ala
|
|
|
ENST00000531203.6:c.1225T>G
|
ENSP00000431975.2:p.Ser409Ala
|
|
|
ENST00000531734.6:c.1336T>G
|
ENSP00000433739.2:p.Ser446Ala
|
|
|
ENST00000652975.2:c.*1169T>G
|
ENSP00000499620.2:n.*1169T>G
|
|
|
ENST00000654851.1:n.1259T>G
|
|
|
|
ENST00000655992.1:c.1225T>G
|
ENSP00000499740.1:p.Ser409Ala
|
|
|
ENST00000659122.2:c.1407+157T>G
|
ENSP00000499621.2:n.1407+157T>G
|
|
|
ENST00000663749.1:c.*1164T>G
|
ENSP00000499739.1:n.*1164T>G
|
|
|
ENST00000667949.2:c.817T>G
|
ENSP00000499465.2:p.Ser273Ala
|
|
|
ENST00000668421.1:c.*1358T>G
|
ENSP00000499362.1:n.*1358T>G
|
|
|
ENST00000679379.1:c.*1169T>G
|
ENSP00000505528.1:n.*1169T>G
|
|
|
ENST00000679593.1:c.1417T>G
|
ENSP00000505999.1:p.Ser473Ala
|
|
|
ENST00000679880.1:n.1953T>G
|
|
|
|
ENST00000679892.1:c.*1185T>G
|
ENSP00000504882.1:n.*1185T>G
|
|
|
ENST00000679981.1:c.*1431T>G
|
ENSP00000506422.1:n.*1431T>G
|
|
|
ENST00000680132.1:c.*1367T>G
|
ENSP00000505950.1:n.*1367T>G
|
|
|
ENST00000680148.1:c.*1169T>G
|
ENSP00000505994.1:n.*1169T>G
|
|
|
ENST00000680170.1:n.2282T>G
|
|
|
|
ENST00000680192.1:n.2375T>G
|
|
|
|
ENST00000680519.1:n.1653T>G
|
|
|
|
ENST00000680531.1:c.*1164T>G
|
ENSP00000506332.1:n.*1164T>G
|
|
|
ENST00000680820.1:c.*1169T>G
|
ENSP00000505735.1:n.*1169T>G
|
|
|
ENST00000680832.1:c.*1517T>G
|
ENSP00000505774.1:n.*1517T>G
|
|
|
ENST00000680929.1:c.*1106T>G
|
ENSP00000504916.1:n.*1106T>G
|
|
|
ENST00000681108.1:c.*1245+157T>G
|
ENSP00000506701.1:n.*1245+157T>G
|
|
|
ENST00000681121.1:c.*527T>G
|
ENSP00000506466.1:n.*527T>G
|
|
|
ENST00000681132.1:c.*1183T>G
|
ENSP00000506195.1:n.*1183T>G
|
|
|
ENST00000681181.1:c.*1402T>G
|
ENSP00000506038.1:n.*1402T>G
|
|
|
ENST00000681218.1:c.*1690T>G
|
ENSP00000505976.1:n.*1690T>G
|
|
|
ENST00000681246.1:c.*1073T>G
|
ENSP00000505534.1:n.*1073T>G
|
|
|
ENST00000681496.1:c.*1690T>G
|
ENSP00000505948.1:n.*1690T>G
|
|
|
ENST00000681834.1:n.1756T>G
|
|
|
|
ENST00000681862.1:c.*1543T>G
|
ENSP00000505537.1:n.*1543T>G
|
|
|
ENST00000256578.7:c.1579T>G
|
ENSP00000256578.3:p.Ser527Ala
|
|
|
ENST00000342115.8:c.1336T>G
|
ENSP00000345498.4:p.Ser446Ala
|
|
|
ENST00000358729.8:c.1354T>G
|
ENSP00000351573.4:p.Ser452Ala
|
|
|
ENST00000369840.6:c.1490T>G
|
|
|
|
ENST00000393688.7:c.1222T>G
|
ENSP00000377292.3:p.Ser408Ala
|
|
|
ENST00000526301.5:n.1618T>G
|
|
|
|
ENST00000528454.5:c.1225T>G
|
ENSP00000437164.1:p.Ser409Ala
|
|
|
ENST00000528667.5:c.1579T>G
|
ENSP00000436541.1:p.Ser527Ala
|
|
|
ENST00000532851.1:n.127T>G
|
|
|
|
ENST00000533132.1:n.119T>G
|
|
|
|
NM_001257360.1:c.1579T>G
|
NP_001244289.1:p.Ser527Ala
|
|
|
NM_001257361.1:c.1225T>G
|
NP_001244290.1:p.Ser409Ala
|
|
|
NM_001308170.1:c.1354T>G
|
NP_001295099.1:p.Ser452Ala
|
|
|
NM_004037.7:c.1579T>G
|
NP_004028.3:p.Ser527Ala
|
|
|
NM_139156.3:c.1336T>G
|
NP_631895.1:p.Ser446Ala
|
|
|
NM_203404.1:c.1222T>G
|
NP_981949.1:p.Ser408Ala
|
|
|
XM_011541247.1:c.1792T>G
|
XP_011539549.1:p.Ser598Ala
|
|
|
XM_011541248.1:c.1782+157T>G
|
XP_011539550.1:n.1782+157T>G
|
|
|
XR_946607.1:n.1815T>G
|
|
|
|
XM_024446431.1:c.1354T>G
|
XP_024302199.1:p.Ser452Ala
|
|
|
XM_024446432.1:c.1430+157T>G
|
XP_024302200.1:n.1430+157T>G
|
|
|
XR_002956282.1:n.1990T>G
|
|
|
|
NM_001257360.2:c.1579T>G
|
NP_001244289.1:p.Ser527Ala
|
|
|
NM_001368809.2:c.1417T>G
MANE Select
|
NP_001355738.1:p.Ser473Ala
|
|
|
NM_004037.9:c.1417T>G
|
NP_004028.4:p.Ser473Ala
|
|
|
NM_001257361.2:c.1225T>G
|
NP_001244290.1:p.Ser409Ala
|
|
|
NM_139156.4:c.1336T>G
|
NP_631895.1:p.Ser446Ala
|
|
