ENST00000321612.8:c.1964C>G
MANE Select
|
ENSP00000370737.4:p.Pro655Arg
|
|
ENST00000460457.2:n.124C>G
|
|
|
ENST00000638233.1:n.399C>G
|
|
|
ENST00000638661.1:c.164C>G
|
ENSP00000491369.1:p.Pro55Arg
|
|
ENST00000638694.1:n.151C>G
|
|
|
ENST00000639318.1:c.164C>G
|
ENSP00000491932.1:p.Pro55Arg
|
|
ENST00000639364.1:n.1664C>G
|
|
|
ENST00000639443.1:n.1532C>G
|
|
|
ENST00000639954.1:n.1672C>G
|
|
|
ENST00000640208.1:c.164C>G
|
ENSP00000491895.1:p.Pro55Arg
|
|
ENST00000640505.1:n.203C>G
|
|
|
ENST00000640592.1:n.1847C>G
|
|
|
ENST00000321612.6:c.1964C>G
|
ENSP00000370737.3:p.Pro655Arg
|
|
ENST00000460457.1:n.103C>G
|
|
|
NM_000170.2:c.1964C>G , LRG_643t1:c.1964C>G
|
NP_000161.2:p.Pro655Arg
|
|
NM_000170.3:c.1964C>G
MANE Select
|
NP_000161.2:p.Pro655Arg
|
|