ENST00000622290.5:c.*405T>G
|
ENSP00000483331.2:n.*405T>G
|
|
ENST00000205557.12:c.4233T>G
MANE Select
|
ENSP00000205557.7:p.Cys1411Trp
|
|
ENST00000640696.1:c.1047T>G
|
ENSP00000492197.1:p.Cys349Trp
|
|
ENST00000205557.11:c.4233T>G
|
ENSP00000205557.7:p.Cys1411Trp
|
|
ENST00000456970.6:c.3858T>G
|
ENSP00000405002.2:n.3858T>G
|
|
ENST00000576204.5:n.1096T>G
|
|
|
ENST00000622290.4:c.*1442T>G
|
ENSP00000483331.1:n.*1442T>G
|
|
NM_001171.5:c.4233T>G
|
NP_001162.4:p.Cys1411Trp
|
|
XM_011522479.1:c.4200T>G
|
XP_011520781.1:p.Cys1400Trp
|
|
XM_011522480.1:c.3891T>G
|
XP_011520782.1:p.Cys1297Trp
|
|
XM_011522481.1:c.3891T>G
|
XP_011520783.1:p.Cys1297Trp
|
|
XR_933134.1:n.538+6458A>C
|
|
|
NM_001351800.1:c.3891T>G
|
NP_001338729.1:p.Cys1297Trp
|
|
NR_147784.1:n.3895T>G
|
|
|
XM_011522479.2:c.4200T>G
|
XP_011520781.1:p.Cys1400Trp
|
|
XM_011522481.3:c.3891T>G
|
XP_011520783.1:p.Cys1297Trp
|
|
XM_017023212.1:c.4065T>G
|
XP_016878701.1:p.Cys1355Trp
|
|
XM_024450261.1:c.4269T>G
|
XP_024306029.1:p.Cys1423Trp
|
|
NM_001171.6:c.4233T>G
MANE Select
|
NP_001162.5:p.Cys1411Trp
|
|