ENST00000622290.5:c.*356G>C
|
ENSP00000483331.2:n.*356G>C
|
|
ENST00000205557.12:c.4184G>C
MANE Select
|
ENSP00000205557.7:p.Cys1395Ser
|
|
ENST00000640696.1:c.998G>C
|
ENSP00000492197.1:p.Cys333Ser
|
|
ENST00000205557.11:c.4184G>C
|
ENSP00000205557.7:p.Cys1395Ser
|
|
ENST00000456970.6:c.3809G>C
|
ENSP00000405002.2:n.3809G>C
|
|
ENST00000576204.5:n.1047G>C
|
|
|
ENST00000622290.4:c.*1393G>C
|
ENSP00000483331.1:n.*1393G>C
|
|
NM_001171.5:c.4184G>C
|
NP_001162.4:p.Cys1395Ser
|
|
XM_011522479.1:c.4151G>C
|
XP_011520781.1:p.Cys1384Ser
|
|
XM_011522480.1:c.3842G>C
|
XP_011520782.1:p.Cys1281Ser
|
|
XM_011522481.1:c.3842G>C
|
XP_011520783.1:p.Cys1281Ser
|
|
XR_933134.1:n.539-5129C>G
|
|
|
NM_001351800.1:c.3842G>C
|
NP_001338729.1:p.Cys1281Ser
|
|
NR_147784.1:n.3846G>C
|
|
|
XM_011522479.2:c.4151G>C
|
XP_011520781.1:p.Cys1384Ser
|
|
XM_011522481.3:c.3842G>C
|
XP_011520783.1:p.Cys1281Ser
|
|
XM_017023212.1:c.4016G>C
|
XP_016878701.1:p.Cys1339Ser
|
|
XM_024450261.1:c.4220G>C
|
XP_024306029.1:p.Cys1407Ser
|
|
NM_001171.6:c.4184G>C
MANE Select
|
NP_001162.5:p.Cys1395Ser
|
|