ENST00000622290.5:c.*392A>G
|
ENSP00000483331.2:n.*392A>G
|
|
ENST00000205557.12:c.4220A>G
MANE Select
|
ENSP00000205557.7:p.Lys1407Arg
|
|
ENST00000640696.1:c.1034A>G
|
ENSP00000492197.1:p.Lys345Arg
|
|
ENST00000205557.11:c.4220A>G
|
ENSP00000205557.7:p.Lys1407Arg
|
|
ENST00000456970.6:c.3845A>G
|
ENSP00000405002.2:n.3845A>G
|
|
ENST00000576204.5:n.1083A>G
|
|
|
ENST00000622290.4:c.*1429A>G
|
ENSP00000483331.1:n.*1429A>G
|
|
NM_001171.5:c.4220A>G
|
NP_001162.4:p.Lys1407Arg
|
|
XM_011522479.1:c.4187A>G
|
XP_011520781.1:p.Lys1396Arg
|
|
XM_011522480.1:c.3878A>G
|
XP_011520782.1:p.Lys1293Arg
|
|
XM_011522481.1:c.3878A>G
|
XP_011520783.1:p.Lys1293Arg
|
|
XR_933134.1:n.538+6471T>C
|
|
|
NM_001351800.1:c.3878A>G
|
NP_001338729.1:p.Lys1293Arg
|
|
NR_147784.1:n.3882A>G
|
|
|
XM_011522479.2:c.4187A>G
|
XP_011520781.1:p.Lys1396Arg
|
|
XM_011522481.3:c.3878A>G
|
XP_011520783.1:p.Lys1293Arg
|
|
XM_017023212.1:c.4052A>G
|
XP_016878701.1:p.Lys1351Arg
|
|
XM_024450261.1:c.4256A>G
|
XP_024306029.1:p.Lys1419Arg
|
|
NM_001171.6:c.4220A>G
MANE Select
|
NP_001162.5:p.Lys1407Arg
|
|