ENST00000394867.9:n.1626C=
|
|
|
ENST00000688002.1:n.3338C=
|
|
|
ENST00000688751.1:n.323C=
|
|
|
ENST00000689792.1:n.1091C=
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|
|
ENST00000262948.10:c.1187C=
MANE Select
|
ENSP00000262948.4:p.Thr396=
|
|
ENST00000262948.9:c.1187C=
|
ENSP00000262948.3:p.Thr396=
|
|
ENST00000394867.8:c.896C=
|
ENSP00000378336.1:p.Thr299=
|
|
ENST00000597263.5:n.372C=
|
|
|
ENST00000599021.1:c.297C=
|
|
|
ENST00000600584.5:n.2636C=
|
|
|
ENST00000601786.5:n.1488C=
|
|
|
NM_030662.3:c.1187C= , LRG_750t1:c.1187C=
|
NP_109587.1:p.Thr396=
|
|
XM_006722799.2:c.908C=
|
XP_006722862.1:p.Thr303=
|
|
XM_011528133.1:c.617C=
|
XP_011526435.1:p.Thr206=
|
|
NM_030662.4:c.1187C=
MANE Select
|
NP_109587.1:p.Thr396=
|
|