ENST00000622290.5:c.*599A>G
|
ENSP00000483331.2:n.*599A>G
|
|
ENST00000205557.12:c.4427A>G
MANE Select
|
ENSP00000205557.7:p.Gln1476Arg
|
|
ENST00000640696.1:c.1241A>G
|
ENSP00000492197.1:p.Gln414Arg
|
|
ENST00000205557.11:c.4427A>G
|
ENSP00000205557.7:p.Gln1476Arg
|
|
ENST00000456970.6:c.4052A>G
|
ENSP00000405002.2:n.4052A>G
|
|
ENST00000576204.5:n.1290A>G
|
|
|
ENST00000622290.4:c.*1636A>G
|
ENSP00000483331.1:n.*1636A>G
|
|
NM_001171.5:c.4427A>G
|
NP_001162.4:p.Gln1476Arg
|
|
XM_011522479.1:c.4394A>G
|
XP_011520781.1:p.Gln1465Arg
|
|
XM_011522480.1:c.4085A>G
|
XP_011520782.1:p.Gln1362Arg
|
|
XM_011522481.1:c.4085A>G
|
XP_011520783.1:p.Gln1362Arg
|
|
XR_933134.1:n.538+5928T>C
|
|
|
NM_001351800.1:c.4085A>G
|
NP_001338729.1:p.Gln1362Arg
|
|
NR_147784.1:n.4089A>G
|
|
|
XM_011522479.2:c.4394A>G
|
XP_011520781.1:p.Gln1465Arg
|
|
XM_011522481.3:c.4085A>G
|
XP_011520783.1:p.Gln1362Arg
|
|
XM_017023212.1:c.4259A>G
|
XP_016878701.1:p.Gln1420Arg
|
|
XM_024450261.1:c.4463A>G
|
XP_024306029.1:p.Gln1488Arg
|
|
NM_001171.6:c.4427A>G
MANE Select
|
NP_001162.5:p.Gln1476Arg
|
|