|
ENST00000684779.1:c.627G=
|
ENSP00000508681.1:p.Ser209=
|
|
|
ENST00000685172.1:c.693G=
|
ENSP00000509604.1:p.Ser231=
|
|
|
ENST00000685763.1:c.546G=
|
ENSP00000509016.1:p.Ser182=
|
|
|
ENST00000686347.1:c.569-5349G=
|
ENSP00000509027.1:n.569-5349G=
|
|
|
ENST00000687191.1:n.1051G=
|
|
|
|
ENST00000689951.1:c.744G=
|
ENSP00000509308.1:p.Ser248=
|
|
|
ENST00000691077.1:c.693G=
|
ENSP00000509843.1:p.Ser231=
|
|
|
ENST00000691576.1:c.569-3115G=
|
ENSP00000510066.1:n.569-3115G=
|
|
|
ENST00000691937.1:c.693G=
|
ENSP00000508768.1:p.Ser231=
|
|
|
ENST00000692487.1:c.693G=
|
ENSP00000509534.1:p.Ser231=
|
|
|
ENST00000692683.1:c.627G=
|
ENSP00000508437.1:p.Ser209=
|
|
|
ENST00000693150.1:c.549G=
|
ENSP00000510309.1:p.Ser183=
|
|
|
ENST00000307102.10:c.693G=
MANE Select
|
ENSP00000302486.5:p.Ser231=
|
|
|
ENST00000307102.9:c.693G=
|
ENSP00000302486.4:p.Ser231=
|
|
|
ENST00000566326.1:c.165G=
|
ENSP00000456438.1:p.Ser55=
|
|
|
NM_002755.3:c.693G= , LRG_725t1:c.693G=
|
NP_002746.1:p.Ser231=
|
|
|
XM_011521783.1:c.627G=
|
XP_011520085.1:p.Ser209=
|
|
|
XM_011521783.3:c.627G=
|
XP_011520085.1:p.Ser209=
|
|
|
XM_017022411.2:c.615G=
|
XP_016877900.1:p.Ser205=
|
|
|
XM_017022412.1:c.549G=
|
XP_016877901.1:p.Ser183=
|
|
|
XM_017022413.1:c.165G=
|
XP_016877902.1:p.Ser55=
|
|
|
NM_002755.4:c.693G=
MANE Select
|
NP_002746.1:p.Ser231=
|
|
