ENST00000622290.5:c.*349T>G
|
ENSP00000483331.2:n.*349T>G
|
|
ENST00000205557.12:c.4177T>G
MANE Select
|
ENSP00000205557.7:p.Tyr1393Asp
|
|
ENST00000640696.1:c.991T>G
|
ENSP00000492197.1:p.Tyr331Asp
|
|
ENST00000205557.11:c.4177T>G
|
ENSP00000205557.7:p.Tyr1393Asp
|
|
ENST00000456970.6:c.3802T>G
|
ENSP00000405002.2:n.3802T>G
|
|
ENST00000576204.5:n.1040T>G
|
|
|
ENST00000622290.4:c.*1386T>G
|
ENSP00000483331.1:n.*1386T>G
|
|
NM_001171.5:c.4177T>G
|
NP_001162.4:p.Tyr1393Asp
|
|
XM_011522479.1:c.4144T>G
|
XP_011520781.1:p.Tyr1382Asp
|
|
XM_011522480.1:c.3835T>G
|
XP_011520782.1:p.Tyr1279Asp
|
|
XM_011522481.1:c.3835T>G
|
XP_011520783.1:p.Tyr1279Asp
|
|
XR_933134.1:n.539-5122A>C
|
|
|
NM_001351800.1:c.3835T>G
|
NP_001338729.1:p.Tyr1279Asp
|
|
NR_147784.1:n.3839T>G
|
|
|
XM_011522479.2:c.4144T>G
|
XP_011520781.1:p.Tyr1382Asp
|
|
XM_011522481.3:c.3835T>G
|
XP_011520783.1:p.Tyr1279Asp
|
|
XM_017023212.1:c.4009T>G
|
XP_016878701.1:p.Tyr1337Asp
|
|
XM_024450261.1:c.4213T>G
|
XP_024306029.1:p.Tyr1405Asp
|
|
NM_001171.6:c.4177T>G
MANE Select
|
NP_001162.5:p.Tyr1393Asp
|
|