ENST00000684779.1:c.*184T>C
(MAP2K1)
|
ENSP00000508681.1:n.*184T>C
|
|
ENST00000685172.1:c.1090T>C
(MAP2K1)
|
ENSP00000509604.1:p.Ser364Pro
|
|
ENST00000685763.1:c.989T>C
(MAP2K1)
|
ENSP00000509016.1:p.Ile330Thr
|
|
ENST00000686347.1:c.809T>C
(MAP2K1)
|
ENSP00000509027.1:p.Ile270Thr
|
|
ENST00000687191.1:n.3416T>C
(MAP2K1)
|
|
|
ENST00000687481.1:n.551T>C
(MAP2K1)
|
|
|
ENST00000688689.1:n.891T>C
(MAP2K1)
|
|
|
ENST00000689951.1:c.1187T>C
(MAP2K1)
|
ENSP00000509308.1:p.Ile396Thr
|
|
ENST00000691077.1:c.*2295T>C
(MAP2K1)
|
ENSP00000509843.1:n.*2295T>C
|
|
ENST00000691576.1:c.1007T>C
(MAP2K1)
|
ENSP00000510066.1:p.Ile336Thr
|
|
ENST00000691937.1:c.*117T>C
(MAP2K1)
|
ENSP00000508768.1:n.*117T>C
|
|
ENST00000692487.1:c.*2736T>C
(MAP2K1)
|
ENSP00000509534.1:n.*2736T>C
|
|
ENST00000692683.1:c.1070T>C
(MAP2K1)
|
ENSP00000508437.1:p.Ile357Thr
|
|
ENST00000693150.1:c.992T>C
(MAP2K1)
|
ENSP00000510309.1:p.Ile331Thr
|
|
ENST00000307102.10:c.1136T>C
(MAP2K1)
MANE Select
|
ENSP00000302486.5:p.Ile379Thr
|
|
ENST00000307102.9:c.1136T>C
(MAP2K1)
|
ENSP00000302486.4:p.Ile379Thr
|
|
ENST00000395589.6:c.*170A>G
(SNAPC5)
|
ENSP00000378954.2:n.*170A>G
|
|
ENST00000563480.6:c.*170A>G
(SNAPC5)
|
ENSP00000457892.1:n.*170A>G
|
|
ENST00000566326.1:c.608T>C
(MAP2K1)
|
ENSP00000456438.1:p.Ile203Thr
|
|
NM_002755.3:c.1136T>C , LRG_725t1:c.1136T>C
(MAP2K1)
|
NP_002746.1:p.Ile379Thr
|
|
NM_006049.2:c.*170A>G
(SNAPC5)
|
NP_006040.1:n.*170A>G
|
|
XM_011521783.1:c.1070T>C
(MAP2K1)
|
XP_011520085.1:p.Ile357Thr
|
|
NM_006049.3:c.*170A>G
(SNAPC5)
|
NP_006040.1:n.*170A>G
|
|
NR_138061.1:n.689A>G
(SNAPC5)
|
|
|
XM_011521783.3:c.1070T>C
(MAP2K1)
|
XP_011520085.1:p.Ile357Thr
|
|
XM_017022411.2:c.1058T>C
(MAP2K1)
|
XP_016877900.1:p.Ile353Thr
|
|
XM_017022412.1:c.992T>C
(MAP2K1)
|
XP_016877901.1:p.Ile331Thr
|
|
XM_017022413.1:c.608T>C
(MAP2K1)
|
XP_016877902.1:p.Ile203Thr
|
|
NM_002755.4:c.1136T>C
(MAP2K1)
MANE Select
|
NP_002746.1:p.Ile379Thr
|
|
NM_006049.4:c.*170A>G
(SNAPC5)
|
NP_006040.1:n.*170A>G
|
|
NR_138061.2:n.636A>G
(SNAPC5)
|
|
|