ENST00000264595.7:c.446C>G
MANE Select
|
ENSP00000264595.2:p.Thr149Ser
|
|
ENST00000264595.6:c.446C>G
|
ENSP00000264595.2:p.Thr149Ser
|
|
ENST00000502310.5:c.101C>G
|
ENSP00000423798.1:p.Thr34Ser
|
|
ENST00000506853.5:n.480C>G
|
|
|
ENST00000510635.1:c.142C>G
|
|
|
ENST00000510955.5:n.367C>G
|
|
|
NM_000027.3:c.446C>G
|
NP_000018.2:p.Thr149Ser
|
|
NM_001171988.1:c.446C>G
|
NP_001165459.1:p.Thr149Ser
|
|
NR_033655.1:n.574C>G
|
|
|
XM_006714123.2:c.446C>G
|
XP_006714186.1:p.Thr149Ser
|
|
XR_001741155.2:n.540C>G
|
|
|
NM_000027.4:c.446C>G
MANE Select
|
NP_000018.2:p.Thr149Ser
|
|
NM_001171988.2:c.446C>G
|
NP_001165459.1:p.Thr149Ser
|
|
NR_033655.2:n.508C>G
|
|
|