ENST00000576204.6:n.780C>G
|
|
|
ENST00000622290.5:c.*89C>G
|
ENSP00000483331.2:n.*89C>G
|
|
ENST00000205557.12:c.3917C>G
MANE Select
|
ENSP00000205557.7:p.Ser1306Cys
|
|
ENST00000640696.1:c.731C>G
|
ENSP00000492197.1:p.Ser244Cys
|
|
ENST00000205557.11:c.3917C>G
|
ENSP00000205557.7:p.Ser1306Cys
|
|
ENST00000456970.6:c.3542C>G
|
ENSP00000405002.2:n.3542C>G
|
|
ENST00000576204.5:n.780C>G
|
|
|
ENST00000622290.4:c.*1126C>G
|
ENSP00000483331.1:n.*1126C>G
|
|
NM_001171.5:c.3917C>G
|
NP_001162.4:p.Ser1306Cys
|
|
XM_011522479.1:c.3884C>G
|
XP_011520781.1:p.Ser1295Cys
|
|
XM_011522480.1:c.3575C>G
|
XP_011520782.1:p.Ser1192Cys
|
|
XM_011522481.1:c.3575C>G
|
XP_011520783.1:p.Ser1192Cys
|
|
XR_932836.1:n.4215C>G
|
|
|
XR_932837.1:n.3953C>G
|
|
|
XR_932838.1:n.4016C>G
|
|
|
XR_933134.1:n.539-4784G>C
|
|
|
NM_001351800.1:c.3575C>G
|
NP_001338729.1:p.Ser1192Cys
|
|
NR_147784.1:n.3579C>G
|
|
|
XM_011522479.2:c.3884C>G
|
XP_011520781.1:p.Ser1295Cys
|
|
XM_011522481.3:c.3575C>G
|
XP_011520783.1:p.Ser1192Cys
|
|
XM_017023212.1:c.3749C>G
|
XP_016878701.1:p.Ser1250Cys
|
|
XM_024450261.1:c.3953C>G
|
XP_024306029.1:p.Ser1318Cys
|
|
XR_932836.2:n.4161C>G
|
|
|
XR_932837.3:n.3898C>G
|
|
|
XR_932838.3:n.3961C>G
|
|
|
NM_001171.6:c.3917C>G
MANE Select
|
NP_001162.5:p.Ser1306Cys
|
|