|
NM_002755.4:c.1177G>A
(MAP2K1)
MANE Select
|
NP_002746.1:p.Val393Ile
|
|
ENST00000307102.10:c.1177G>A
(MAP2K1)
MANE Select
|
ENSP00000302486.5:p.Val393Ile
|
|
NM_002755.3:c.1177G>A , LRG_725t1:c.1177G>A
(MAP2K1)
|
NP_002746.1:p.Val393Ile
|
|
NM_006049.2:c.*129C>T
(SNAPC5)
|
NP_006040.1:n.*129C>T
|
|
NM_006049.3:c.*129C>T
(SNAPC5)
|
NP_006040.1:n.*129C>T
|
|
NM_006049.4:c.*129C>T
(SNAPC5)
|
NP_006040.1:n.*129C>T
|
|
NR_138061.1:n.648C>T
(SNAPC5)
|
|
|
NR_138061.2:n.595C>T
(SNAPC5)
|
|
|
ENST00000307102.9:c.1177G>A
(MAP2K1)
|
ENSP00000302486.4:p.Val393Ile
|
|
ENST00000395589.6:c.*129C>T
(SNAPC5)
|
ENSP00000378954.2:n.*129C>T
|
|
ENST00000563480.6:c.*129C>T
(SNAPC5)
|
ENSP00000457892.1:n.*129C>T
|
|
ENST00000566326.1:c.649G>A
(MAP2K1)
|
ENSP00000456438.1:p.Val217Ile
|
|
ENST00000684779.1:c.*225G>A
(MAP2K1)
|
ENSP00000508681.1:n.*225G>A
|
|
ENST00000685172.1:c.1131G>A
(MAP2K1)
|
ENSP00000509604.1:p.Ala377=
|
|
ENST00000685763.1:c.1030G>A
(MAP2K1)
|
ENSP00000509016.1:p.Val344Ile
|
|
ENST00000686347.1:c.850G>A
(MAP2K1)
|
ENSP00000509027.1:p.Val284Ile
|
|
ENST00000687191.1:n.3457G>A
(MAP2K1)
|
|
|
ENST00000687481.1:n.592G>A
(MAP2K1)
|
|
|
ENST00000688689.1:n.932G>A
(MAP2K1)
|
|
|
ENST00000689951.1:c.1228G>A
(MAP2K1)
|
ENSP00000509308.1:p.Val410Ile
|
|
ENST00000691077.1:c.*2336G>A
(MAP2K1)
|
ENSP00000509843.1:n.*2336G>A
|
|
ENST00000691576.1:c.1048G>A
(MAP2K1)
|
ENSP00000510066.1:p.Val350Ile
|
|
ENST00000691937.1:c.*158G>A
(MAP2K1)
|
ENSP00000508768.1:n.*158G>A
|
|
ENST00000692487.1:c.*2777G>A
(MAP2K1)
|
ENSP00000509534.1:n.*2777G>A
|
|
ENST00000692683.1:c.1111G>A
(MAP2K1)
|
ENSP00000508437.1:p.Val371Ile
|
|
ENST00000693150.1:c.1033G>A
(MAP2K1)
|
ENSP00000510309.1:p.Val345Ile
|
|
XM_011521783.1:c.1111G>A
(MAP2K1)
|
XP_011520085.1:p.Val371Ile
|
|
XM_011521783.3:c.1111G>A
(MAP2K1)
|
XP_011520085.1:p.Val371Ile
|
|
XM_017022411.2:c.1099G>A
(MAP2K1)
|
XP_016877900.1:p.Val367Ile
|
|
XM_017022412.1:c.1033G>A
(MAP2K1)
|
XP_016877901.1:p.Val345Ile
|
|
XM_017022413.1:c.649G>A
(MAP2K1)
|
XP_016877902.1:p.Val217Ile
|
