ENST00000576204.6:n.959C>G
|
|
|
ENST00000622290.5:c.*268C>G
|
ENSP00000483331.2:n.*268C>G
|
|
ENST00000205557.12:c.4096C>G
MANE Select
|
ENSP00000205557.7:p.His1366Asp
|
|
ENST00000640696.1:c.910C>G
|
ENSP00000492197.1:p.His304Asp
|
|
ENST00000205557.11:c.4096C>G
|
ENSP00000205557.7:p.His1366Asp
|
|
ENST00000456970.6:c.3721C>G
|
ENSP00000405002.2:n.3721C>G
|
|
ENST00000576204.5:n.959C>G
|
|
|
ENST00000622290.4:c.*1305C>G
|
ENSP00000483331.1:n.*1305C>G
|
|
NM_001171.5:c.4096C>G
|
NP_001162.4:p.His1366Asp
|
|
XM_011522479.1:c.4063C>G
|
XP_011520781.1:p.His1355Asp
|
|
XM_011522480.1:c.3754C>G
|
XP_011520782.1:p.His1252Asp
|
|
XM_011522481.1:c.3754C>G
|
XP_011520783.1:p.His1252Asp
|
|
XR_933134.1:n.539-5041G>C
|
|
|
NM_001351800.1:c.3754C>G
|
NP_001338729.1:p.His1252Asp
|
|
NR_147784.1:n.3758C>G
|
|
|
XM_011522479.2:c.4063C>G
|
XP_011520781.1:p.His1355Asp
|
|
XM_011522481.3:c.3754C>G
|
XP_011520783.1:p.His1252Asp
|
|
XM_017023212.1:c.3928C>G
|
XP_016878701.1:p.His1310Asp
|
|
XM_024450261.1:c.4132C>G
|
XP_024306029.1:p.His1378Asp
|
|
NM_001171.6:c.4096C>G
MANE Select
|
NP_001162.5:p.His1366Asp
|
|