|
ENST00000394867.9:n.1630C=
|
|
|
|
ENST00000688002.1:n.3342C=
|
|
|
|
ENST00000688751.1:n.327C=
|
|
|
|
ENST00000689792.1:n.1095C=
|
|
|
|
ENST00000262948.10:c.1191C=
MANE Select
|
ENSP00000262948.4:p.Arg397=
|
|
|
ENST00000262948.9:c.1191C=
|
ENSP00000262948.3:p.Arg397=
|
|
|
ENST00000394867.8:c.900C=
|
ENSP00000378336.1:p.Arg300=
|
|
|
ENST00000597263.5:n.376C=
|
|
|
|
ENST00000599021.1:c.301C=
|
|
|
|
ENST00000600584.5:n.2640C=
|
|
|
|
ENST00000601786.5:n.1492C=
|
|
|
|
NM_030662.3:c.1191C= , LRG_750t1:c.1191C=
|
NP_109587.1:p.Arg397=
|
|
|
XM_006722799.2:c.912C=
|
XP_006722862.1:p.Arg304=
|
|
|
XM_011528133.1:c.621C=
|
XP_011526435.1:p.Arg207=
|
|
|
NM_030662.4:c.1191C=
MANE Select
|
NP_109587.1:p.Arg397=
|
|
