ENST00000622290.5:c.*383T>A
|
ENSP00000483331.2:n.*383T>A
|
|
ENST00000205557.12:c.4211T>A
MANE Select
|
ENSP00000205557.7:p.Val1404Glu
|
|
ENST00000640696.1:c.1025T>A
|
ENSP00000492197.1:p.Val342Glu
|
|
ENST00000205557.11:c.4211T>A
|
ENSP00000205557.7:p.Val1404Glu
|
|
ENST00000456970.6:c.3836T>A
|
ENSP00000405002.2:n.3836T>A
|
|
ENST00000576204.5:n.1074T>A
|
|
|
ENST00000622290.4:c.*1420T>A
|
ENSP00000483331.1:n.*1420T>A
|
|
NM_001171.5:c.4211T>A
|
NP_001162.4:p.Val1404Glu
|
|
XM_011522479.1:c.4178T>A
|
XP_011520781.1:p.Val1393Glu
|
|
XM_011522480.1:c.3869T>A
|
XP_011520782.1:p.Val1290Glu
|
|
XM_011522481.1:c.3869T>A
|
XP_011520783.1:p.Val1290Glu
|
|
XR_933134.1:n.538+6480A>T
|
|
|
NM_001351800.1:c.3869T>A
|
NP_001338729.1:p.Val1290Glu
|
|
NR_147784.1:n.3873T>A
|
|
|
XM_011522479.2:c.4178T>A
|
XP_011520781.1:p.Val1393Glu
|
|
XM_011522481.3:c.3869T>A
|
XP_011520783.1:p.Val1290Glu
|
|
XM_017023212.1:c.4043T>A
|
XP_016878701.1:p.Val1348Glu
|
|
XM_024450261.1:c.4247T>A
|
XP_024306029.1:p.Val1416Glu
|
|
NM_001171.6:c.4211T>A
MANE Select
|
NP_001162.5:p.Val1404Glu
|
|