ENST00000688602.1:c.1062T>G
|
|
|
ENST00000689936.1:c.1044T>G
|
|
|
ENST00000359596.8:c.12652T>G
MANE Select
|
ENSP00000352608.2:p.Phe4218Val
|
|
ENST00000355481.8:c.12637T>G
|
ENSP00000347667.3:p.Phe4213Val
|
|
ENST00000359596.7:c.12652T>G
|
ENSP00000352608.2:p.Phe4218Val
|
|
ENST00000360985.7:c.12634T>G
|
ENSP00000354254.4:p.Phe4212Val
|
|
ENST00000594335.5:c.6021T>G
|
|
|
NM_000540.2:c.12652T>G , LRG_766t1:c.12652T>G
|
NP_000531.2:p.Phe4218Val
|
|
NM_001042723.1:c.12637T>G
|
NP_001036188.1:p.Phe4213Val
|
|
XM_006723317.1:c.12634T>G
|
XP_006723380.1:p.Phe4212Val
|
|
XM_006723319.1:c.12619T>G
|
XP_006723382.1:p.Phe4207Val
|
|
XM_011527204.1:c.12649T>G
|
XP_011525506.1:p.Phe4217Val
|
|
XM_011527205.1:c.12652T>G
|
XP_011525507.1:p.Phe4218Val
|
|
XM_006723317.2:c.12634T>G
|
XP_006723380.1:p.Phe4212Val
|
|
XM_006723319.2:c.12619T>G
|
XP_006723382.1:p.Phe4207Val
|
|
XM_011527205.2:c.12652T>G
|
XP_011525507.1:p.Phe4218Val
|
|
NM_000540.3:c.12652T>G
MANE Select
|
NP_000531.2:p.Phe4218Val
|
|
NM_001042723.2:c.12637T>G
|
NP_001036188.1:p.Phe4213Val
|
|