ENST00000388996.10:c.905C>G
MANE Select
|
ENSP00000373648.3:p.Thr302Ser
|
|
ENST00000521134.6:c.545C>G
|
ENSP00000429799.1:p.Thr182Ser
|
|
ENST00000638588.1:c.578C>G
|
ENSP00000491940.1:p.Thr193Ser
|
|
ENST00000639358.1:c.555C>G
|
|
|
ENST00000639496.1:c.578C>G
|
ENSP00000491165.1:p.Thr193Ser
|
|
ENST00000388996.8:c.905C>G
|
ENSP00000373648.3:p.Thr302Ser
|
|
ENST00000519445.5:c.905C>G
|
ENSP00000428790.1:p.Thr302Ser
|
|
ENST00000519589.1:n.683C>G
|
|
|
ENST00000521134.5:c.545C>G
|
ENSP00000429799.1:p.Thr182Ser
|
|
ENST00000621976.1:c.542C>G
|
ENSP00000482510.1:p.Thr181Ser
|
|
NM_001204824.1:c.545C>G
|
NP_001191753.1:p.Thr182Ser
|
|
NM_004519.3:c.905C>G
|
NP_004510.1:p.Thr302Ser
|
|
XM_005250914.2:c.-252C>G
|
XP_005250971.1:n.-252C>G
|
|
XM_006716555.2:c.197C>G
|
XP_006716618.1:p.Thr66Ser
|
|
XM_011517026.1:c.545C>G
|
XP_011515328.1:p.Thr182Ser
|
|
XM_005250914.3:c.-252C>G
|
XP_005250971.1:n.-252C>G
|
|
XM_006716555.3:c.197C>G
|
XP_006716618.1:p.Thr66Ser
|
|
XM_011517026.2:c.545C>G
|
XP_011515328.1:p.Thr182Ser
|
|
XM_017013400.1:c.683C>G
|
XP_016868889.1:p.Thr228Ser
|
|
NM_004519.4:c.905C>G
MANE Select
|
NP_004510.1:p.Thr302Ser
|
|
NM_001204824.2:c.545C>G
|
NP_001191753.1:p.Thr182Ser
|
|