ENST00000371375.2:c.4462T>G
|
ENSP00000360426.1:p.Ser1488Ala
|
|
ENST00000685253.1:c.*1929T>G
|
ENSP00000509405.1:n.*1929T>G
|
|
ENST00000685889.1:n.2121T>G
|
|
|
ENST00000686807.1:n.805T>G
|
|
|
ENST00000686954.1:c.*670T>G
|
ENSP00000508416.1:n.*670T>G
|
|
ENST00000688810.1:c.4414T>G
|
ENSP00000509140.1:p.Ser1472Ala
|
|
ENST00000689233.1:n.9594T>G
|
|
|
ENST00000690340.1:n.3059T>G
|
|
|
ENST00000692286.1:c.5254T>G
|
ENSP00000509490.1:p.Ser1752Ala
|
|
ENST00000692396.1:c.5338T>G
|
ENSP00000508605.1:p.Ser1780Ala
|
|
ENST00000371380.8:c.5386T>G
MANE Select
|
ENSP00000360431.2:p.Ser1796Ala
|
|
ENST00000371385.8:c.4360T>G
|
ENSP00000360438.4:p.Ser1454Ala
|
|
ENST00000674738.1:c.3941T>G
|
|
|
ENST00000674827.1:c.3502T>G
|
ENSP00000502523.1:p.Ser1168Ala
|
|
ENST00000675218.1:c.4462T>G
|
ENSP00000501910.1:p.Ser1488Ala
|
|
ENST00000675487.1:c.*1319T>G
|
ENSP00000502340.1:n.*1319T>G
|
|
ENST00000675718.1:c.4655T>G
|
|
|
ENST00000260766.7:c.5386T>G
|
ENSP00000260766.3:p.Ser1796Ala
|
|
ENST00000371375.1:c.4462T>G
|
ENSP00000360426.1:p.Ser1488Ala
|
|
ENST00000371380.7:c.5386T>G
|
ENSP00000360431.2:p.Ser1796Ala
|
|
ENST00000371385.7:c.4462T>G
|
ENSP00000360438.3:p.Ser1488Ala
|
|
NM_001165979.2:c.4462T>G
|
NP_001159451.1:p.Ser1488Ala
|
|
NM_001288989.1:c.5338T>G
|
NP_001275918.1:p.Ser1780Ala
|
|
NM_016341.3:c.5386T>G
|
NP_057425.3:p.Ser1796Ala
|
|
XM_006717885.2:c.5428T>G
|
XP_006717948.1:p.Ser1810Ala
|
|
XM_006717886.2:c.5428T>G
|
XP_006717949.1:p.Ser1810Ala
|
|
XM_006717888.2:c.5425T>G
|
XP_006717951.1:p.Ser1809Ala
|
|
XM_006717889.2:c.5380T>G
|
XP_006717952.1:p.Ser1794Ala
|
|
XM_006717890.1:c.4504T>G
|
XP_006717953.1:p.Ser1502Ala
|
|
XM_011539849.1:c.5428T>G
|
XP_011538151.1:p.Ser1810Ala
|
|
XM_011539850.1:c.4273T>G
|
XP_011538152.1:p.Ser1425Ala
|
|
XM_006717885.4:c.5428T>G
|
XP_006717948.1:p.Ser1810Ala
|
|
XM_006717888.4:c.5425T>G
|
XP_006717951.1:p.Ser1809Ala
|
|
XM_006717889.4:c.5380T>G
|
XP_006717952.1:p.Ser1794Ala
|
|
XM_006717890.3:c.4504T>G
|
XP_006717953.1:p.Ser1502Ala
|
|
XM_011539849.3:c.5428T>G
|
XP_011538151.1:p.Ser1810Ala
|
|
XM_011539850.3:c.4273T>G
|
XP_011538152.1:p.Ser1425Ala
|
|
XM_017016310.2:c.5428T>G
|
XP_016871799.1:p.Ser1810Ala
|
|
XM_017016311.2:c.5428T>G
|
XP_016871800.1:p.Ser1810Ala
|
|
XM_017016312.2:c.4414T>G
|
XP_016871801.1:p.Ser1472Ala
|
|
NM_001288989.2:c.5338T>G
|
NP_001275918.1:p.Ser1780Ala
|
|
NM_016341.4:c.5386T>G
MANE Select
|
NP_057425.3:p.Ser1796Ala
|
|