ENST00000699485.1:c.433A=
|
ENSP00000514396.1:p.Thr145=
|
|
ENST00000362057.4:c.2089A=
MANE Select
|
ENSP00000354623.3:p.Thr697=
|
|
ENST00000674036.8:c.1062A=
|
|
|
ENST00000674048.1:n.1970A=
|
|
|
ENST00000265134.10:c.940A=
|
ENSP00000265134.6:p.Thr314=
|
|
ENST00000362057.3:c.2089A=
|
ENSP00000354623.3:p.Thr697=
|
|
ENST00000374059.7:c.1036A=
|
ENSP00000363172.3:p.Thr346=
|
|
NM_001083885.2:c.940A=
|
NP_001077354.2:p.Thr314=
|
|
NM_001173425.1:c.2089A=
|
NP_001166896.1:p.Thr697=
|
|
NM_015404.3:c.2089A=
|
NP_056219.3:p.Thr697=
|
|
XM_005251897.3:c.1426A=
|
XP_005251954.2:p.Thr476=
|
|
XM_011518484.1:c.2122A=
|
XP_011516786.1:p.Thr708=
|
|
XM_011518485.1:c.2122A=
|
XP_011516787.1:p.Thr708=
|
|
XM_011518486.1:c.2122A=
|
XP_011516788.1:p.Thr708=
|
|
XM_011518487.1:c.1996A=
|
XP_011516789.1:p.Thr666=
|
|
XM_011518488.1:c.1879A=
|
XP_011516790.1:p.Thr627=
|
|
XM_011518495.1:c.799A=
|
XP_011516797.1:p.Thr267=
|
|
XR_929747.1:n.3026A=
|
|
|
XR_929748.1:n.2924A=
|
|
|
NM_001346890.1:c.1036A=
|
NP_001333819.1:p.Thr346=
|
|
XM_011518486.2:c.2122A=
|
XP_011516788.1:p.Thr708=
|
|
XM_011518487.2:c.1996A=
|
XP_011516789.1:p.Thr666=
|
|
XM_011518488.2:c.1879A=
|
XP_011516790.1:p.Thr627=
|
|
XR_929747.2:n.2337A=
|
|
|
XR_929748.2:n.2235A=
|
|
|
NM_015404.4:c.2089A=
MANE Select
|
NP_056219.3:p.Thr697=
|
|
NM_001173425.2:c.2089A=
|
NP_001166896.1:p.Thr697=
|
|
NM_001083885.3:c.940A=
|
NP_001077354.2:p.Thr314=
|
|