ENST00000684779.1:c.628-2226C>T
|
ENSP00000508681.1:n.628-2226C>T
|
|
ENST00000685172.1:c.706C>T
|
ENSP00000509604.1:p.Gln236Ter
|
|
ENST00000685763.1:c.559C>T
|
ENSP00000509016.1:p.Gln187Ter
|
|
ENST00000686347.1:c.569-2226C>T
|
ENSP00000509027.1:n.569-2226C>T
|
|
ENST00000687191.1:n.1064C>T
|
|
|
ENST00000687481.1:n.121C>T
|
|
|
ENST00000689951.1:c.757C>T
|
ENSP00000509308.1:p.Gln253Ter
|
|
ENST00000691077.1:c.702C>T
|
ENSP00000509843.1:p.Ser234=
|
|
ENST00000691576.1:c.577C>T
|
ENSP00000510066.1:p.Gln193Ter
|
|
ENST00000691937.1:c.706C>T
|
ENSP00000508768.1:p.Gln236Ter
|
|
ENST00000692487.1:c.702C>T
|
ENSP00000509534.1:p.Ser234=
|
|
ENST00000692683.1:c.640C>T
|
ENSP00000508437.1:p.Gln214Ter
|
|
ENST00000693150.1:c.562C>T
|
ENSP00000510309.1:p.Gln188Ter
|
|
ENST00000307102.10:c.706C>T
MANE Select
|
ENSP00000302486.5:p.Gln236Ter
|
|
ENST00000307102.9:c.706C>T
|
ENSP00000302486.4:p.Gln236Ter
|
|
ENST00000566326.1:c.178C>T
|
ENSP00000456438.1:p.Gln60Ter
|
|
NM_002755.3:c.706C>T , LRG_725t1:c.706C>T
|
NP_002746.1:p.Gln236Ter
|
|
XM_011521783.1:c.640C>T
|
XP_011520085.1:p.Gln214Ter
|
|
XM_011521783.3:c.640C>T
|
XP_011520085.1:p.Gln214Ter
|
|
XM_017022411.2:c.628C>T
|
XP_016877900.1:p.Gln210Ter
|
|
XM_017022412.1:c.562C>T
|
XP_016877901.1:p.Gln188Ter
|
|
XM_017022413.1:c.178C>T
|
XP_016877902.1:p.Gln60Ter
|
|
NM_002755.4:c.706C>T
MANE Select
|
NP_002746.1:p.Gln236Ter
|
|