ENST00000622290.5:c.*403T>G
|
ENSP00000483331.2:n.*403T>G
|
|
ENST00000205557.12:c.4231T>G
MANE Select
|
ENSP00000205557.7:p.Cys1411Gly
|
|
ENST00000640696.1:c.1045T>G
|
ENSP00000492197.1:p.Cys349Gly
|
|
ENST00000205557.11:c.4231T>G
|
ENSP00000205557.7:p.Cys1411Gly
|
|
ENST00000456970.6:c.3856T>G
|
ENSP00000405002.2:n.3856T>G
|
|
ENST00000576204.5:n.1094T>G
|
|
|
ENST00000622290.4:c.*1440T>G
|
ENSP00000483331.1:n.*1440T>G
|
|
NM_001171.5:c.4231T>G
|
NP_001162.4:p.Cys1411Gly
|
|
XM_011522479.1:c.4198T>G
|
XP_011520781.1:p.Cys1400Gly
|
|
XM_011522480.1:c.3889T>G
|
XP_011520782.1:p.Cys1297Gly
|
|
XM_011522481.1:c.3889T>G
|
XP_011520783.1:p.Cys1297Gly
|
|
XR_933134.1:n.538+6460A>C
|
|
|
NM_001351800.1:c.3889T>G
|
NP_001338729.1:p.Cys1297Gly
|
|
NR_147784.1:n.3893T>G
|
|
|
XM_011522479.2:c.4198T>G
|
XP_011520781.1:p.Cys1400Gly
|
|
XM_011522481.3:c.3889T>G
|
XP_011520783.1:p.Cys1297Gly
|
|
XM_017023212.1:c.4063T>G
|
XP_016878701.1:p.Cys1355Gly
|
|
XM_024450261.1:c.4267T>G
|
XP_024306029.1:p.Cys1423Gly
|
|
NM_001171.6:c.4231T>G
MANE Select
|
NP_001162.5:p.Cys1411Gly
|
|