ENST00000642498.1:c.984G>T
|
ENSP00000493631.1:p.Val328=
|
|
ENST00000642538.1:c.*328G>T
|
ENSP00000493927.1:n.*328G>T
|
|
ENST00000643188.1:c.984G>T
|
ENSP00000493903.1:p.Val328=
|
|
ENST00000643443.1:c.*691G>T
|
ENSP00000495572.1:n.*691G>T
|
|
ENST00000643502.1:c.641G>T
|
|
|
ENST00000643908.1:n.1202G>T
|
|
|
ENST00000644538.1:n.1261G>T
|
|
|
ENST00000644793.1:c.984G>T
|
ENSP00000495750.1:p.Val328=
|
|
ENST00000645328.1:c.362G>T
|
|
|
ENST00000645408.1:c.517G>T
|
|
|
ENST00000645723.1:n.2223G>T
|
|
|
ENST00000646405.1:c.*402G>T
|
ENSP00000493744.1:n.*402G>T
|
|
ENST00000646512.1:n.1130G>T
|
|
|
ENST00000646735.1:c.651G>T
|
ENSP00000493763.1:p.Val217=
|
|
ENST00000651619.1:c.984G>T
MANE Select
|
ENSP00000498303.1:p.Val328=
|
|
ENST00000216951.6:c.984G>T
|
ENSP00000216951.2:p.Val328=
|
|
ENST00000451957.2:c.651G>T
|
ENSP00000407517.2:p.Val217=
|
|
NM_000178.2:c.984G>T
|
NP_000169.1:p.Val328=
|
|
XM_005260406.3:c.984G>T
|
XP_005260463.1:p.Val328=
|
|
XM_011528796.1:c.984G>T
|
XP_011527098.1:p.Val328=
|
|
NM_000178.4:c.984G>T
MANE Select
|
NP_000169.1:p.Val328=
|
|
NM_001322494.1:c.984G>T
|
NP_001309423.1:p.Val328=
|
|
NM_001322495.1:c.984G>T
|
NP_001309424.1:p.Val328=
|
|