ENST00000688602.1:c.381T>G
|
|
|
ENST00000689936.1:c.363T>G
|
|
|
ENST00000359596.8:c.11971T>G
MANE Select
|
ENSP00000352608.2:p.Phe3991Val
|
|
ENST00000355481.8:c.11956T>G
|
ENSP00000347667.3:p.Phe3986Val
|
|
ENST00000359596.7:c.11971T>G
|
ENSP00000352608.2:p.Phe3991Val
|
|
ENST00000360985.7:c.11953T>G
|
ENSP00000354254.4:p.Phe3985Val
|
|
ENST00000593322.1:c.580T>G
|
|
|
ENST00000594335.5:c.5340T>G
|
|
|
NM_000540.2:c.11971T>G , LRG_766t1:c.11971T>G
|
NP_000531.2:p.Phe3991Val
|
|
NM_001042723.1:c.11956T>G
|
NP_001036188.1:p.Phe3986Val
|
|
XM_006723317.1:c.11953T>G
|
XP_006723380.1:p.Phe3985Val
|
|
XM_006723319.1:c.11938T>G
|
XP_006723382.1:p.Phe3980Val
|
|
XM_011527204.1:c.11968T>G
|
XP_011525506.1:p.Phe3990Val
|
|
XM_011527205.1:c.11971T>G
|
XP_011525507.1:p.Phe3991Val
|
|
XM_006723317.2:c.11953T>G
|
XP_006723380.1:p.Phe3985Val
|
|
XM_006723319.2:c.11938T>G
|
XP_006723382.1:p.Phe3980Val
|
|
XM_011527205.2:c.11971T>G
|
XP_011525507.1:p.Phe3991Val
|
|
NM_000540.3:c.11971T>G
MANE Select
|
NP_000531.2:p.Phe3991Val
|
|
NM_001042723.2:c.11956T>G
|
NP_001036188.1:p.Phe3986Val
|
|