ENST00000622290.5:c.*503T>A
|
ENSP00000483331.2:n.*503T>A
|
|
ENST00000205557.12:c.4331T>A
MANE Select
|
ENSP00000205557.7:p.Leu1444His
|
|
ENST00000640696.1:c.1145T>A
|
ENSP00000492197.1:p.Leu382His
|
|
ENST00000205557.11:c.4331T>A
|
ENSP00000205557.7:p.Leu1444His
|
|
ENST00000456970.6:c.3956T>A
|
ENSP00000405002.2:n.3956T>A
|
|
ENST00000576204.5:n.1194T>A
|
|
|
ENST00000622290.4:c.*1540T>A
|
ENSP00000483331.1:n.*1540T>A
|
|
NM_001171.5:c.4331T>A
|
NP_001162.4:p.Leu1444His
|
|
XM_011522479.1:c.4298T>A
|
XP_011520781.1:p.Leu1433His
|
|
XM_011522480.1:c.3989T>A
|
XP_011520782.1:p.Leu1330His
|
|
XM_011522481.1:c.3989T>A
|
XP_011520783.1:p.Leu1330His
|
|
XR_933134.1:n.538+6360A>T
|
|
|
NM_001351800.1:c.3989T>A
|
NP_001338729.1:p.Leu1330His
|
|
NR_147784.1:n.3993T>A
|
|
|
XM_011522479.2:c.4298T>A
|
XP_011520781.1:p.Leu1433His
|
|
XM_011522481.3:c.3989T>A
|
XP_011520783.1:p.Leu1330His
|
|
XM_017023212.1:c.4163T>A
|
XP_016878701.1:p.Leu1388His
|
|
XM_024450261.1:c.4367T>A
|
XP_024306029.1:p.Leu1456His
|
|
NM_001171.6:c.4331T>A
MANE Select
|
NP_001162.5:p.Leu1444His
|
|