|
ENST00000684779.1:c.*182C=
(MAP2K1)
|
ENSP00000508681.1:n.*182C=
|
|
|
ENST00000685172.1:c.1088C=
(MAP2K1)
|
ENSP00000509604.1:p.Pro363=
|
|
|
ENST00000685763.1:c.987C=
(MAP2K1)
|
ENSP00000509016.1:p.Thr329=
|
|
|
ENST00000686347.1:c.807C=
(MAP2K1)
|
ENSP00000509027.1:p.Thr269=
|
|
|
ENST00000687191.1:n.3414C=
(MAP2K1)
|
|
|
|
ENST00000687481.1:n.549C=
(MAP2K1)
|
|
|
|
ENST00000688689.1:n.889C=
(MAP2K1)
|
|
|
|
ENST00000689951.1:c.1185C=
(MAP2K1)
|
ENSP00000509308.1:p.Thr395=
|
|
|
ENST00000691077.1:c.*2293C=
(MAP2K1)
|
ENSP00000509843.1:n.*2293C=
|
|
|
ENST00000691576.1:c.1005C=
(MAP2K1)
|
ENSP00000510066.1:p.Thr335=
|
|
|
ENST00000691937.1:c.*115C=
(MAP2K1)
|
ENSP00000508768.1:n.*115C=
|
|
|
ENST00000692487.1:c.*2734C=
(MAP2K1)
|
ENSP00000509534.1:n.*2734C=
|
|
|
ENST00000692683.1:c.1068C=
(MAP2K1)
|
ENSP00000508437.1:p.Thr356=
|
|
|
ENST00000693150.1:c.990C=
(MAP2K1)
|
ENSP00000510309.1:p.Thr330=
|
|
|
ENST00000307102.10:c.1134C=
(MAP2K1)
MANE Select
|
ENSP00000302486.5:p.Thr378=
|
|
|
ENST00000307102.9:c.1134C=
(MAP2K1)
|
ENSP00000302486.4:p.Thr378=
|
|
|
ENST00000395589.6:c.*172G=
(SNAPC5)
|
ENSP00000378954.2:n.*172G=
|
|
|
ENST00000563480.6:c.*172G=
(SNAPC5)
|
ENSP00000457892.1:n.*172G=
|
|
|
ENST00000566326.1:c.606C=
(MAP2K1)
|
ENSP00000456438.1:p.Thr202=
|
|
|
NM_002755.3:c.1134C= , LRG_725t1:c.1134C=
(MAP2K1)
|
NP_002746.1:p.Thr378=
|
|
|
NM_006049.2:c.*172G=
(SNAPC5)
|
NP_006040.1:n.*172G=
|
|
|
XM_011521783.1:c.1068C=
(MAP2K1)
|
XP_011520085.1:p.Thr356=
|
|
|
NM_006049.3:c.*172G=
(SNAPC5)
|
NP_006040.1:n.*172G=
|
|
|
NR_138061.1:n.691G=
(SNAPC5)
|
|
|
|
XM_011521783.3:c.1068C=
(MAP2K1)
|
XP_011520085.1:p.Thr356=
|
|
|
XM_017022411.2:c.1056C=
(MAP2K1)
|
XP_016877900.1:p.Thr352=
|
|
|
XM_017022412.1:c.990C=
(MAP2K1)
|
XP_016877901.1:p.Thr330=
|
|
|
XM_017022413.1:c.606C=
(MAP2K1)
|
XP_016877902.1:p.Thr202=
|
|
|
NM_002755.4:c.1134C=
(MAP2K1)
MANE Select
|
NP_002746.1:p.Thr378=
|
|
|
NM_006049.4:c.*172G=
(SNAPC5)
|
NP_006040.1:n.*172G=
|
|
|
NR_138061.2:n.638G=
(SNAPC5)
|
|
|
