ENST00000576204.6:n.765C>G
|
|
|
ENST00000622290.5:c.*74C>G
|
ENSP00000483331.2:n.*74C>G
|
|
ENST00000205557.12:c.3902C>G
MANE Select
|
ENSP00000205557.7:p.Thr1301Ser
|
|
ENST00000640696.1:c.716C>G
|
ENSP00000492197.1:p.Thr239Ser
|
|
ENST00000205557.11:c.3902C>G
|
ENSP00000205557.7:p.Thr1301Ser
|
|
ENST00000456970.6:c.3527C>G
|
ENSP00000405002.2:n.3527C>G
|
|
ENST00000576204.5:n.765C>G
|
|
|
ENST00000622290.4:c.*1111C>G
|
ENSP00000483331.1:n.*1111C>G
|
|
NM_001171.5:c.3902C>G
|
NP_001162.4:p.Thr1301Ser
|
|
XM_011522479.1:c.3869C>G
|
XP_011520781.1:p.Thr1290Ser
|
|
XM_011522480.1:c.3560C>G
|
XP_011520782.1:p.Thr1187Ser
|
|
XM_011522481.1:c.3560C>G
|
XP_011520783.1:p.Thr1187Ser
|
|
XR_932836.1:n.4200C>G
|
|
|
XR_932837.1:n.3938C>G
|
|
|
XR_932838.1:n.4001C>G
|
|
|
XR_933134.1:n.539-4769G>C
|
|
|
NM_001351800.1:c.3560C>G
|
NP_001338729.1:p.Thr1187Ser
|
|
NR_147784.1:n.3564C>G
|
|
|
XM_011522479.2:c.3869C>G
|
XP_011520781.1:p.Thr1290Ser
|
|
XM_011522481.3:c.3560C>G
|
XP_011520783.1:p.Thr1187Ser
|
|
XM_017023212.1:c.3734C>G
|
XP_016878701.1:p.Thr1245Ser
|
|
XM_024450261.1:c.3938C>G
|
XP_024306029.1:p.Thr1313Ser
|
|
XR_932836.2:n.4146C>G
|
|
|
XR_932837.3:n.3883C>G
|
|
|
XR_932838.3:n.3946C>G
|
|
|
NM_001171.6:c.3902C>G
MANE Select
|
NP_001162.5:p.Thr1301Ser
|
|