|
ENST00000394867.9:n.1815C=
|
|
|
|
ENST00000688751.1:n.512C=
|
|
|
|
ENST00000689792.1:n.1280C=
|
|
|
|
ENST00000262948.10:c.*173C=
MANE Select
|
ENSP00000262948.4:n.*173C=
|
|
|
ENST00000262948.9:c.*173C=
|
ENSP00000262948.3:n.*173C=
|
|
|
ENST00000394867.8:c.*173C=
|
ENSP00000378336.1:n.*173C=
|
|
|
ENST00000600584.5:n.2825C=
|
|
|
|
ENST00000601786.5:n.1677C=
|
|
|
|
NM_030662.3:c.*173C= , LRG_750t1:c.*173C=
|
NP_109587.1:n.*173C=
|
|
|
XM_006722799.2:c.*173C=
|
XP_006722862.1:n.*173C=
|
|
|
XM_011528133.1:c.*173C=
|
XP_011526435.1:n.*173C=
|
|
|
NM_030662.4:c.*173C=
MANE Select
|
NP_109587.1:n.*173C=
|
|
