ENST00000394867.9:n.1457C=
|
|
|
ENST00000688002.1:n.3169C=
|
|
|
ENST00000688751.1:n.154C=
|
|
|
ENST00000689792.1:n.922C=
|
|
|
ENST00000262948.10:c.1018C=
MANE Select
|
ENSP00000262948.4:p.Pro340=
|
|
ENST00000262948.9:c.1018C=
|
ENSP00000262948.3:p.Pro340=
|
|
ENST00000394867.8:c.727C=
|
ENSP00000378336.1:p.Pro243=
|
|
ENST00000595715.1:n.833C=
|
|
|
ENST00000597263.5:n.203C=
|
|
|
ENST00000599021.1:c.128C=
|
|
|
ENST00000600584.5:n.1578C=
|
|
|
ENST00000601786.5:n.1319C=
|
|
|
NM_030662.3:c.1018C= , LRG_750t1:c.1018C=
|
NP_109587.1:p.Pro340=
|
|
XM_006722799.2:c.739C=
|
XP_006722862.1:p.Pro247=
|
|
XM_011528133.1:c.448C=
|
XP_011526435.1:p.Pro150=
|
|
XM_017026989.1:c.1018C=
|
XP_016882478.1:p.Pro340=
|
|
XM_017026990.1:c.739C=
|
XP_016882479.1:p.Pro247=
|
|
NM_030662.4:c.1018C=
MANE Select
|
NP_109587.1:p.Pro340=
|
|