ENST00000684779.1:c.*133A>T
(MAP2K1)
|
ENSP00000508681.1:n.*133A>T
|
|
ENST00000685172.1:c.1039A>T
(MAP2K1)
|
ENSP00000509604.1:p.Arg347Ter
|
|
ENST00000685763.1:c.938A>T
(MAP2K1)
|
ENSP00000509016.1:p.Lys313Met
|
|
ENST00000686347.1:c.758A>T
(MAP2K1)
|
ENSP00000509027.1:p.Lys253Met
|
|
ENST00000687191.1:n.3365A>T
(MAP2K1)
|
|
|
ENST00000687481.1:n.500A>T
(MAP2K1)
|
|
|
ENST00000688689.1:n.840A>T
(MAP2K1)
|
|
|
ENST00000689951.1:c.1136A>T
(MAP2K1)
|
ENSP00000509308.1:p.Lys379Met
|
|
ENST00000691077.1:c.*2244A>T
(MAP2K1)
|
ENSP00000509843.1:n.*2244A>T
|
|
ENST00000691576.1:c.956A>T
(MAP2K1)
|
ENSP00000510066.1:p.Lys319Met
|
|
ENST00000691937.1:c.*66A>T
(MAP2K1)
|
ENSP00000508768.1:n.*66A>T
|
|
ENST00000692487.1:c.*2685A>T
(MAP2K1)
|
ENSP00000509534.1:n.*2685A>T
|
|
ENST00000692683.1:c.1019A>T
(MAP2K1)
|
ENSP00000508437.1:p.Lys340Met
|
|
ENST00000693150.1:c.941A>T
(MAP2K1)
|
ENSP00000510309.1:p.Lys314Met
|
|
ENST00000307102.10:c.1085A>T
(MAP2K1)
MANE Select
|
ENSP00000302486.5:p.Lys362Met
|
|
ENST00000307102.9:c.1085A>T
(MAP2K1)
|
ENSP00000302486.4:p.Lys362Met
|
|
ENST00000395589.6:c.*221T>A
(SNAPC5)
|
ENSP00000378954.2:n.*221T>A
|
|
ENST00000563480.6:c.*221T>A
(SNAPC5)
|
ENSP00000457892.1:n.*221T>A
|
|
ENST00000566326.1:c.557A>T
(MAP2K1)
|
ENSP00000456438.1:p.Lys186Met
|
|
NM_002755.3:c.1085A>T , LRG_725t1:c.1085A>T
(MAP2K1)
|
NP_002746.1:p.Lys362Met
|
|
NM_006049.2:c.*221T>A
(SNAPC5)
|
NP_006040.1:n.*221T>A
|
|
XM_011521783.1:c.1019A>T
(MAP2K1)
|
XP_011520085.1:p.Lys340Met
|
|
NM_006049.3:c.*221T>A
(SNAPC5)
|
NP_006040.1:n.*221T>A
|
|
NR_138061.1:n.740T>A
(SNAPC5)
|
|
|
XM_011521783.3:c.1019A>T
(MAP2K1)
|
XP_011520085.1:p.Lys340Met
|
|
XM_017022411.2:c.1007A>T
(MAP2K1)
|
XP_016877900.1:p.Lys336Met
|
|
XM_017022412.1:c.941A>T
(MAP2K1)
|
XP_016877901.1:p.Lys314Met
|
|
XM_017022413.1:c.557A>T
(MAP2K1)
|
XP_016877902.1:p.Lys186Met
|
|
NM_002755.4:c.1085A>T
(MAP2K1)
MANE Select
|
NP_002746.1:p.Lys362Met
|
|
NM_006049.4:c.*221T>A
(SNAPC5)
|
NP_006040.1:n.*221T>A
|
|
NR_138061.2:n.687T>A
(SNAPC5)
|
|
|