ENST00000236671.7:c.1165T>G
MANE Select
|
ENSP00000236671.2:p.Phe389Val
|
|
ENST00000367196.4:c.1060T>G
|
ENSP00000356164.4:p.Phe354Val
|
|
ENST00000427721.3:c.590T>G
|
|
|
ENST00000429746.2:c.1060T>G
|
ENSP00000402586.2:p.Phe354Val
|
|
ENST00000433655.6:c.*331T>G
|
ENSP00000404902.1:n.*331T>G
|
|
ENST00000438213.6:c.1282T>G
|
ENSP00000415036.2:p.Phe428Val
|
|
ENST00000636397.1:c.1071+226T>G
|
ENSP00000489910.1:n.1071+226T>G
|
|
ENST00000636571.1:c.1144T>G
|
ENSP00000490770.1:p.Phe382Val
|
|
ENST00000636579.1:c.72+226T>G
|
ENSP00000490489.1:n.72+226T>G
|
|
ENST00000636615.1:c.1071+226T>G
|
ENSP00000490014.1:n.1071+226T>G
|
|
ENST00000636843.1:c.1159T>G
|
ENSP00000490897.1:p.Phe387Val
|
|
ENST00000637158.1:n.763T>G
|
|
|
ENST00000637381.2:n.3593T>G
|
|
|
ENST00000637387.1:c.1144T>G
|
ENSP00000490598.1:p.Phe382Val
|
|
ENST00000637815.2:c.1147T>G
|
ENSP00000490344.1:p.Phe383Val
|
|
ENST00000637915.1:c.1156T>G
|
ENSP00000490471.1:p.Phe386Val
|
|
ENST00000637937.1:n.473T>G
|
|
|
ENST00000678991.1:c.*1026T>G
|
ENSP00000503019.1:n.*1026T>G
|
|
ENST00000236671.6:c.1165T>G
|
ENSP00000236671.2:p.Phe389Val
|
|
ENST00000427721.2:c.471+226T>G
|
ENSP00000415840.2:n.471+226T>G
|
|
ENST00000429746.1:c.496T>G
|
ENSP00000402586.1:p.Phe166Val
|
|
ENST00000433655.5:c.*331T>G
|
ENSP00000404902.1:n.*331T>G
|
|
NM_001909.4:c.1165T>G
|
NP_001900.1:p.Phe389Val
|
|
NM_001909.5:c.1165T>G
MANE Select
|
NP_001900.1:p.Phe389Val
|
|