ENST00000261201.10:c.4644C>A
|
ENSP00000261201.4:p.Asn1548Lys
|
|
ENST00000682426.1:n.2089+818C>A
|
|
|
ENST00000682879.1:c.*3610+818C>A
|
ENSP00000508210.1:n.*3610+818C>A
|
|
ENST00000683105.1:c.*536+818C>A
|
ENSP00000506801.1:n.*536+818C>A
|
|
ENST00000683676.1:c.4212-6042C>A
|
ENSP00000508167.1:n.4212-6042C>A
|
|
ENST00000683695.1:n.977+818C>A
|
|
|
ENST00000684084.1:c.4461+818C>A
|
ENSP00000507859.1:n.4461+818C>A
|
|
ENST00000261200.9:c.4512+818C>A
MANE Select
|
ENSP00000261200.4:n.4512+818C>A
|
|
ENST00000261201.9:c.4644C>A
|
ENSP00000261201.4:p.Asn1548Lys
|
|
ENST00000261200.8:c.4512+818C>A
|
ENSP00000261200.4:n.4512+818C>A
|
|
ENST00000261201.8:c.4644C>A
|
ENSP00000261201.4:p.Asn1548Lys
|
|
ENST00000544039.5:c.3525C>A
|
ENSP00000440521.1:p.Asn1175Lys
|
|
NM_005691.3:c.4644C>A
|
NP_005682.2:p.Asn1548Lys
|
|
NM_020297.3:c.4512+818C>A
|
NP_064693.2:n.4512+818C>A
|
|
XM_005253284.2:c.4512+818C>A
|
XP_005253341.1:n.4512+818C>A
|
|
XM_005253286.2:c.4512+818C>A
|
XP_005253343.1:n.4512+818C>A
|
|
XM_005253287.3:c.4644C>A
|
XP_005253344.1:p.Asn1548Lys
|
|
XM_005253288.2:c.4512+818C>A
|
XP_005253345.1:n.4512+818C>A
|
|
XM_005253289.2:c.4473+818C>A
|
XP_005253346.1:n.4473+818C>A
|
|
XM_005253290.2:c.4371+818C>A
|
XP_005253347.1:n.4371+818C>A
|
|
XM_006719025.2:c.4605C>A
|
XP_006719088.1:p.Asn1535Lys
|
|
XM_011520545.1:c.4512+818C>A
|
XP_011518847.1:n.4512+818C>A
|
|
XR_931420.1:n.632-22030G>T
|
|
|
XR_931421.1:n.632-22030G>T
|
|
|
XR_931422.1:n.306-22030G>T
|
|
|
XM_005253284.4:c.4512+818C>A
|
XP_005253341.1:n.4512+818C>A
|
|
XM_005253286.4:c.4512+818C>A
|
XP_005253343.1:n.4512+818C>A
|
|
XM_005253287.5:c.4644C>A
|
XP_005253344.1:p.Asn1548Lys
|
|
XM_005253288.4:c.4512+818C>A
|
XP_005253345.1:n.4512+818C>A
|
|
XM_005253289.4:c.4473+818C>A
|
XP_005253346.1:n.4473+818C>A
|
|
XM_005253290.4:c.4371+818C>A
|
XP_005253347.1:n.4371+818C>A
|
|
XM_006719025.4:c.4605C>A
|
XP_006719088.1:p.Asn1535Lys
|
|
XM_011520545.3:c.4512+818C>A
|
XP_011518847.1:n.4512+818C>A
|
|
XR_931420.3:n.632-22030G>T
|
|
|
XR_931422.2:n.318-22030G>T
|
|
|
NM_001377273.1:c.4512+818C>A
|
NP_001364202.1:n.4512+818C>A
|
|
NM_001377274.1:c.3645+818C>A
|
NP_001364203.1:n.3645+818C>A
|
|
NM_005691.4:c.4644C>A
|
NP_005682.2:p.Asn1548Lys
|
|
NM_020297.4:c.4512+818C>A
MANE Select
|
NP_064693.2:n.4512+818C>A
|
|