|
ENST00000684779.1:c.628-2083G=
|
ENSP00000508681.1:n.628-2083G=
|
|
|
ENST00000685172.1:c.849G=
|
ENSP00000509604.1:p.Ala283=
|
|
|
ENST00000685763.1:c.702G=
|
ENSP00000509016.1:p.Ala234=
|
|
|
ENST00000686347.1:c.569-2083G=
|
ENSP00000509027.1:n.569-2083G=
|
|
|
ENST00000687191.1:n.1207G=
|
|
|
|
ENST00000687481.1:n.264G=
|
|
|
|
ENST00000689951.1:c.900G=
|
ENSP00000509308.1:p.Ala300=
|
|
|
ENST00000691077.1:c.*86G=
|
ENSP00000509843.1:n.*86G=
|
|
|
ENST00000691576.1:c.720G=
|
ENSP00000510066.1:p.Ala240=
|
|
|
ENST00000691937.1:c.849G=
|
ENSP00000508768.1:p.Ala283=
|
|
|
ENST00000692487.1:c.*86G=
|
ENSP00000509534.1:n.*86G=
|
|
|
ENST00000692683.1:c.783G=
|
ENSP00000508437.1:p.Ala261=
|
|
|
ENST00000693150.1:c.705G=
|
ENSP00000510309.1:p.Ala235=
|
|
|
ENST00000307102.10:c.849G=
MANE Select
|
ENSP00000302486.5:p.Ala283=
|
|
|
ENST00000307102.9:c.849G=
|
ENSP00000302486.4:p.Ala283=
|
|
|
ENST00000566326.1:c.321G=
|
ENSP00000456438.1:p.Ala107=
|
|
|
NM_002755.3:c.849G= , LRG_725t1:c.849G=
|
NP_002746.1:p.Ala283=
|
|
|
XM_011521783.1:c.783G=
|
XP_011520085.1:p.Ala261=
|
|
|
XM_011521783.3:c.783G=
|
XP_011520085.1:p.Ala261=
|
|
|
XM_017022411.2:c.771G=
|
XP_016877900.1:p.Ala257=
|
|
|
XM_017022412.1:c.705G=
|
XP_016877901.1:p.Ala235=
|
|
|
XM_017022413.1:c.321G=
|
XP_016877902.1:p.Ala107=
|
|
|
NM_002755.4:c.849G=
MANE Select
|
NP_002746.1:p.Ala283=
|
|
