ENST00000371375.2:c.4423C>T
|
ENSP00000360426.1:p.Gln1475Ter
|
|
ENST00000685253.1:c.*1890C>T
|
ENSP00000509405.1:n.*1890C>T
|
|
ENST00000685889.1:n.2082C>T
|
|
|
ENST00000686807.1:n.766C>T
|
|
|
ENST00000686954.1:c.*631C>T
|
ENSP00000508416.1:n.*631C>T
|
|
ENST00000688810.1:c.4375C>T
|
ENSP00000509140.1:p.Gln1459Ter
|
|
ENST00000689233.1:n.9555C>T
|
|
|
ENST00000690340.1:n.3020C>T
|
|
|
ENST00000692286.1:c.5215C>T
|
ENSP00000509490.1:p.Gln1739Ter
|
|
ENST00000692396.1:c.5299C>T
|
ENSP00000508605.1:p.Gln1767Ter
|
|
ENST00000371380.8:c.5347C>T
MANE Select
|
ENSP00000360431.2:p.Gln1783Ter
|
|
ENST00000371385.8:c.4321C>T
|
ENSP00000360438.4:p.Gln1441Ter
|
|
ENST00000674738.1:c.3902C>T
|
|
|
ENST00000674827.1:c.3463C>T
|
ENSP00000502523.1:p.Gln1155Ter
|
|
ENST00000675218.1:c.4423C>T
|
ENSP00000501910.1:p.Gln1475Ter
|
|
ENST00000675487.1:c.*1280C>T
|
ENSP00000502340.1:n.*1280C>T
|
|
ENST00000675718.1:c.4616C>T
|
|
|
ENST00000260766.7:c.5347C>T
|
ENSP00000260766.3:p.Gln1783Ter
|
|
ENST00000371375.1:c.4423C>T
|
ENSP00000360426.1:p.Gln1475Ter
|
|
ENST00000371380.7:c.5347C>T
|
ENSP00000360431.2:p.Gln1783Ter
|
|
ENST00000371385.7:c.4423C>T
|
ENSP00000360438.3:p.Gln1475Ter
|
|
NM_001165979.2:c.4423C>T
|
NP_001159451.1:p.Gln1475Ter
|
|
NM_001288989.1:c.5299C>T
|
NP_001275918.1:p.Gln1767Ter
|
|
NM_016341.3:c.5347C>T
|
NP_057425.3:p.Gln1783Ter
|
|
XM_006717885.2:c.5389C>T
|
XP_006717948.1:p.Gln1797Ter
|
|
XM_006717886.2:c.5389C>T
|
XP_006717949.1:p.Gln1797Ter
|
|
XM_006717888.2:c.5386C>T
|
XP_006717951.1:p.Gln1796Ter
|
|
XM_006717889.2:c.5341C>T
|
XP_006717952.1:p.Gln1781Ter
|
|
XM_006717890.1:c.4465C>T
|
XP_006717953.1:p.Gln1489Ter
|
|
XM_011539849.1:c.5389C>T
|
XP_011538151.1:p.Gln1797Ter
|
|
XM_011539850.1:c.4234C>T
|
XP_011538152.1:p.Gln1412Ter
|
|
XM_006717885.4:c.5389C>T
|
XP_006717948.1:p.Gln1797Ter
|
|
XM_006717888.4:c.5386C>T
|
XP_006717951.1:p.Gln1796Ter
|
|
XM_006717889.4:c.5341C>T
|
XP_006717952.1:p.Gln1781Ter
|
|
XM_006717890.3:c.4465C>T
|
XP_006717953.1:p.Gln1489Ter
|
|
XM_011539849.3:c.5389C>T
|
XP_011538151.1:p.Gln1797Ter
|
|
XM_011539850.3:c.4234C>T
|
XP_011538152.1:p.Gln1412Ter
|
|
XM_017016310.2:c.5389C>T
|
XP_016871799.1:p.Gln1797Ter
|
|
XM_017016311.2:c.5389C>T
|
XP_016871800.1:p.Gln1797Ter
|
|
XM_017016312.2:c.4375C>T
|
XP_016871801.1:p.Gln1459Ter
|
|
NM_001288989.2:c.5299C>T
|
NP_001275918.1:p.Gln1767Ter
|
|
NM_016341.4:c.5347C>T
MANE Select
|
NP_057425.3:p.Gln1783Ter
|
|