ENST00000344686.8:c.2298G>A
(MAP3K14)
MANE Select
|
ENSP00000478552.1:p.Pro766=
|
|
ENST00000586644.2:n.1235G>A
(MAP3K14)
|
|
|
ENST00000617331.3:c.2298G>A
(MAP3K14)
|
ENSP00000480974.3:p.Pro766=
|
|
ENST00000680632.1:c.1352G>A
(MAP3K14)
|
ENSP00000505027.1:n.1352G>A
|
|
ENST00000344686.6:c.2298G>A
(MAP3K14)
|
ENSP00000478552.1:p.Pro766=
|
|
ENST00000376926.8:c.2298G>A
(MAP3K14)
|
ENSP00000482657.1:p.Pro766=
|
|
ENST00000592267.1:n.1105G>A
(MAP3K14)
|
|
|
NM_003954.4:c.2298G>A
(MAP3K14)
|
NP_003945.2:p.Pro766=
|
|
NR_024434.2:n.295+106C>T
(MAP3K14-AS1)
|
|
|
NR_024435.2:n.749+106C>T
(MAP3K14-AS1)
|
|
|
NR_110324.1:n.480+106C>T
(MAP3K14-AS1)
|
|
|
NR_110325.1:n.475+106C>T
(MAP3K14-AS1)
|
|
|
NR_110326.1:n.379+106C>T
(MAP3K14-AS1)
|
|
|
XM_011525441.1:c.2298G>A
(MAP3K14)
|
XP_011523743.1:p.Pro766=
|
|
XR_934591.1:n.2613G>A
(MAP3K14)
|
|
|
NM_003954.5:c.2298G>A
(MAP3K14)
MANE Select
|
NP_003945.2:p.Pro766=
|
|
XM_011525441.2:c.2298G>A
(MAP3K14)
|
XP_011523743.1:p.Pro766=
|
|