ENST00000321612.8:c.2139G>T
MANE Select
|
ENSP00000370737.4:p.Val713=
|
|
ENST00000638233.1:n.574G>T
|
|
|
ENST00000638661.1:c.339G>T
|
ENSP00000491369.1:p.Val113=
|
|
ENST00000638694.1:n.326G>T
|
|
|
ENST00000639318.1:c.339G>T
|
ENSP00000491932.1:p.Val113=
|
|
ENST00000639364.1:n.1839G>T
|
|
|
ENST00000639443.1:n.1707G>T
|
|
|
ENST00000639954.1:n.1847G>T
|
|
|
ENST00000640505.1:n.378G>T
|
|
|
ENST00000321612.6:c.2139G>T
|
ENSP00000370737.3:p.Val713=
|
|
NM_000170.2:c.2139G>T , LRG_643t1:c.2139G>T
|
NP_000161.2:p.Val713=
|
|
NM_000170.3:c.2139G>T
MANE Select
|
NP_000161.2:p.Val713=
|
|