|
ENST00000367698.4:c.1254C=
MANE Select
|
ENSP00000356671.3:p.Thr418=
|
|
|
ENST00000367698.3:c.1254C=
|
ENSP00000356671.3:p.Thr418=
|
|
|
ENST00000617423.4:c.639C=
|
ENSP00000478688.1:p.Thr213=
|
|
|
NM_000488.3:c.1254C= , LRG_577t1:c.1254C=
|
NP_000479.1:p.Thr418=
|
|
|
XM_005245198.2:c.1110C=
|
XP_005245255.1:p.Thr370=
|
|
|
NM_001365052.1:c.1110C=
|
NP_001351981.1:p.Thr370=
|
|
|
NM_000488.4:c.1254C=
MANE Select
|
NP_000479.1:p.Thr418=
|
|
|
NM_001365052.2:c.1110C=
|
NP_001351981.1:p.Thr370=
|
|
|
NM_001386302.1:c.1377C=
|
NP_001373231.1:p.Thr459=
|
|
|
NM_001386303.1:c.1335C=
|
NP_001373232.1:p.Thr445=
|
|
|
NM_001386304.1:c.1233C=
|
NP_001373233.1:p.Thr411=
|
|
|
NM_001386305.1:c.1197C=
|
NP_001373234.1:p.Thr399=
|
|
|
NM_001386306.1:c.1038C=
|
NP_001373235.1:p.Thr346=
|
|
