ENST00000336079.8:c.1070C>G
MANE Select
|
ENSP00000336725.3:p.Pro357Arg
|
|
ENST00000336079.7:c.1070C>G
|
ENSP00000336725.3:p.Pro357Arg
|
|
ENST00000360160.8:c.1070C>G
|
ENSP00000353284.4:p.Pro357Arg
|
|
ENST00000495478.1:n.185C>G
|
|
|
NM_001122665.2:c.1070C>G
|
NP_001116137.1:p.Pro357Arg
|
|
NM_001302552.1:c.1061C>G
|
NP_001289481.1:p.Pro354Arg
|
|
NM_004660.4:c.1070C>G
|
NP_004651.2:p.Pro357Arg
|
|
XM_006724878.1:c.1070C>G
|
XP_006724941.1:p.Pro357Arg
|
|
XM_011531471.1:c.1070C>G
|
XP_011529773.1:p.Pro357Arg
|
|
NM_001122665.3:c.1070C>G
|
NP_001116137.1:p.Pro357Arg
|
|
NM_001302552.2:c.1061C>G
|
NP_001289481.1:p.Pro354Arg
|
|
NM_001324195.1:c.1070C>G
|
NP_001311124.1:p.Pro357Arg
|
|
NR_136716.1:n.1539C>G
|
|
|
NR_136717.1:n.1301C>G
|
|
|
NR_136718.1:n.1619C>G
|
|
|
NR_136719.1:n.1409C>G
|
|
|
NR_136720.1:n.1539C>G
|
|
|
NR_136721.1:n.1132C>G
|
|
|
NR_136722.1:n.1216C>G
|
|
|
NR_136723.1:n.1534C>G
|
|
|
NR_136724.1:n.1454C>G
|
|
|
XR_001756014.2:n.1174C>G
|
|
|
NM_004660.5:c.1070C>G
MANE Select
|
NP_004651.2:p.Pro357Arg
|
|
NM_001302552.3:c.1061C>G
|
NP_001289481.1:p.Pro354Arg
|
|
NM_001324195.2:c.1070C>G
|
NP_001311124.1:p.Pro357Arg
|
|
NR_136716.2:n.1457C>G
|
|
|
NR_136717.2:n.1219C>G
|
|
|
NR_136718.2:n.1537C>G
|
|
|
NR_136719.2:n.1327C>G
|
|
|
NR_136720.2:n.1457C>G
|
|
|
NR_136721.2:n.1122C>G
|
|
|