ENST00000388996.10:c.812C>T
MANE Select
|
ENSP00000373648.3:p.Thr271Ile
|
|
ENST00000521134.6:c.452C>T
|
ENSP00000429799.1:p.Thr151Ile
|
|
ENST00000638588.1:c.485C>T
|
ENSP00000491940.1:p.Thr162Ile
|
|
ENST00000639358.1:c.462C>T
|
|
|
ENST00000639496.1:c.485C>T
|
ENSP00000491165.1:p.Thr162Ile
|
|
ENST00000388996.8:c.812C>T
|
ENSP00000373648.3:p.Thr271Ile
|
|
ENST00000519445.5:c.812C>T
|
ENSP00000428790.1:p.Thr271Ile
|
|
ENST00000519589.1:n.590C>T
|
|
|
ENST00000521134.5:c.452C>T
|
ENSP00000429799.1:p.Thr151Ile
|
|
ENST00000621976.1:c.449C>T
|
ENSP00000482510.1:p.Thr150Ile
|
|
NM_001204824.1:c.452C>T
|
NP_001191753.1:p.Thr151Ile
|
|
NM_004519.3:c.812C>T
|
NP_004510.1:p.Thr271Ile
|
|
XM_005250914.2:c.-345C>T
|
XP_005250971.1:n.-345C>T
|
|
XM_006716555.2:c.104C>T
|
XP_006716618.1:p.Thr35Ile
|
|
XM_011517026.1:c.452C>T
|
XP_011515328.1:p.Thr151Ile
|
|
XM_005250914.3:c.-345C>T
|
XP_005250971.1:n.-345C>T
|
|
XM_006716555.3:c.104C>T
|
XP_006716618.1:p.Thr35Ile
|
|
XM_011517026.2:c.452C>T
|
XP_011515328.1:p.Thr151Ile
|
|
XM_017013400.1:c.590C>T
|
XP_016868889.1:p.Thr197Ile
|
|
NM_004519.4:c.812C>T
MANE Select
|
NP_004510.1:p.Thr271Ile
|
|
NM_001204824.2:c.452C>T
|
NP_001191753.1:p.Thr151Ile
|
|