ENST00000261201.10:c.4580G>C
|
ENSP00000261201.4:p.Cys1527Ser
|
|
ENST00000682426.1:n.2089+754G>C
|
|
|
ENST00000682879.1:c.*3610+754G>C
|
ENSP00000508210.1:n.*3610+754G>C
|
|
ENST00000683105.1:c.*536+754G>C
|
ENSP00000506801.1:n.*536+754G>C
|
|
ENST00000683676.1:c.4212-6106G>C
|
ENSP00000508167.1:n.4212-6106G>C
|
|
ENST00000683695.1:n.977+754G>C
|
|
|
ENST00000684084.1:c.4461+754G>C
|
ENSP00000507859.1:n.4461+754G>C
|
|
ENST00000261200.9:c.4512+754G>C
MANE Select
|
ENSP00000261200.4:n.4512+754G>C
|
|
ENST00000261201.9:c.4580G>C
|
ENSP00000261201.4:p.Cys1527Ser
|
|
ENST00000261200.8:c.4512+754G>C
|
ENSP00000261200.4:n.4512+754G>C
|
|
ENST00000261201.8:c.4580G>C
|
ENSP00000261201.4:p.Cys1527Ser
|
|
ENST00000544039.5:c.3461G>C
|
ENSP00000440521.1:p.Cys1154Ser
|
|
NM_005691.3:c.4580G>C
|
NP_005682.2:p.Cys1527Ser
|
|
NM_020297.3:c.4512+754G>C
|
NP_064693.2:n.4512+754G>C
|
|
XM_005253284.2:c.4512+754G>C
|
XP_005253341.1:n.4512+754G>C
|
|
XM_005253286.2:c.4512+754G>C
|
XP_005253343.1:n.4512+754G>C
|
|
XM_005253287.3:c.4580G>C
|
XP_005253344.1:p.Cys1527Ser
|
|
XM_005253288.2:c.4512+754G>C
|
XP_005253345.1:n.4512+754G>C
|
|
XM_005253289.2:c.4473+754G>C
|
XP_005253346.1:n.4473+754G>C
|
|
XM_005253290.2:c.4371+754G>C
|
XP_005253347.1:n.4371+754G>C
|
|
XM_006719025.2:c.4541G>C
|
XP_006719088.1:p.Cys1514Ser
|
|
XM_011520545.1:c.4512+754G>C
|
XP_011518847.1:n.4512+754G>C
|
|
XR_931420.1:n.632-21966C>G
|
|
|
XR_931421.1:n.632-21966C>G
|
|
|
XR_931422.1:n.306-21966C>G
|
|
|
XM_005253284.4:c.4512+754G>C
|
XP_005253341.1:n.4512+754G>C
|
|
XM_005253286.4:c.4512+754G>C
|
XP_005253343.1:n.4512+754G>C
|
|
XM_005253287.5:c.4580G>C
|
XP_005253344.1:p.Cys1527Ser
|
|
XM_005253288.4:c.4512+754G>C
|
XP_005253345.1:n.4512+754G>C
|
|
XM_005253289.4:c.4473+754G>C
|
XP_005253346.1:n.4473+754G>C
|
|
XM_005253290.4:c.4371+754G>C
|
XP_005253347.1:n.4371+754G>C
|
|
XM_006719025.4:c.4541G>C
|
XP_006719088.1:p.Cys1514Ser
|
|
XM_011520545.3:c.4512+754G>C
|
XP_011518847.1:n.4512+754G>C
|
|
XR_931420.3:n.632-21966C>G
|
|
|
XR_931422.2:n.318-21966C>G
|
|
|
NM_001377273.1:c.4512+754G>C
|
NP_001364202.1:n.4512+754G>C
|
|
NM_001377274.1:c.3645+754G>C
|
NP_001364203.1:n.3645+754G>C
|
|
NM_005691.4:c.4580G>C
|
NP_005682.2:p.Cys1527Ser
|
|
NM_020297.4:c.4512+754G>C
MANE Select
|
NP_064693.2:n.4512+754G>C
|
|