ENST00000321612.8:c.2001T>G
MANE Select
|
ENSP00000370737.4:p.Pro667=
|
|
ENST00000460457.2:n.161T>G
|
|
|
ENST00000638233.1:n.436T>G
|
|
|
ENST00000638661.1:c.201T>G
|
ENSP00000491369.1:p.Pro67=
|
|
ENST00000638694.1:n.188T>G
|
|
|
ENST00000639318.1:c.201T>G
|
ENSP00000491932.1:p.Pro67=
|
|
ENST00000639364.1:n.1701T>G
|
|
|
ENST00000639443.1:n.1569T>G
|
|
|
ENST00000639954.1:n.1709T>G
|
|
|
ENST00000640208.1:c.201T>G
|
ENSP00000491895.1:p.Pro67=
|
|
ENST00000640505.1:n.240T>G
|
|
|
ENST00000640592.1:n.1884T>G
|
|
|
ENST00000321612.6:c.2001T>G
|
ENSP00000370737.3:p.Pro667=
|
|
ENST00000460457.1:n.140T>G
|
|
|
NM_000170.2:c.2001T>G , LRG_643t1:c.2001T>G
|
NP_000161.2:p.Pro667=
|
|
NM_000170.3:c.2001T>G
MANE Select
|
NP_000161.2:p.Pro667=
|
|