ENST00000321612.8:c.2052+12C>T
MANE Select
|
ENSP00000370737.4:n.2052+12C>T
|
|
ENST00000460457.2:n.212+12C>T
|
|
|
ENST00000638233.1:n.487+12C>T
|
|
|
ENST00000638661.1:c.252+12C>T
|
ENSP00000491369.1:n.252+12C>T
|
|
ENST00000638694.1:n.239+12C>T
|
|
|
ENST00000639318.1:c.252+12C>T
|
ENSP00000491932.1:n.252+12C>T
|
|
ENST00000639364.1:n.1752+12C>T
|
|
|
ENST00000639443.1:n.1620+12C>T
|
|
|
ENST00000639954.1:n.1760+12C>T
|
|
|
ENST00000640208.1:c.264C>T
|
ENSP00000491895.1:p.Phe88=
|
|
ENST00000640505.1:n.291+12C>T
|
|
|
ENST00000640592.1:n.1947C>T
|
|
|
ENST00000321612.6:c.2052+12C>T
|
ENSP00000370737.3:n.2052+12C>T
|
|
ENST00000460457.1:n.203C>T
|
|
|
NM_000170.2:c.2052+12C>T , LRG_643t1:c.2052+12C>T
|
NP_000161.2:n.2052+12C>T
|
|
NM_000170.3:c.2052+12C>T
MANE Select
|
NP_000161.2:n.2052+12C>T
|
|