ENST00000593677.2:c.1685T>G
|
|
|
ENST00000688602.1:c.3082T>G
|
|
|
ENST00000689936.1:c.3054T>G
|
|
|
ENST00000692547.1:n.142T>G
|
|
|
ENST00000359596.8:c.14749T>G
MANE Select
|
ENSP00000352608.2:p.Phe4917Val
|
|
ENST00000355481.8:c.14734T>G
|
ENSP00000347667.3:p.Phe4912Val
|
|
ENST00000359596.7:c.14749T>G
|
ENSP00000352608.2:p.Phe4917Val
|
|
ENST00000360985.7:c.14731T>G
|
ENSP00000354254.4:p.Phe4911Val
|
|
NM_000540.2:c.14749T>G , LRG_766t1:c.14749T>G
|
NP_000531.2:p.Phe4917Val
|
|
NM_001042723.1:c.14734T>G
|
NP_001036188.1:p.Phe4912Val
|
|
XM_006723317.1:c.14731T>G
|
XP_006723380.1:p.Phe4911Val
|
|
XM_006723319.1:c.14716T>G
|
XP_006723382.1:p.Phe4906Val
|
|
XM_011527204.1:c.14746T>G
|
XP_011525506.1:p.Phe4916Val
|
|
XM_011527205.1:c.14662T>G
|
XP_011525507.1:p.Phe4888Val
|
|
XM_006723317.2:c.14731T>G
|
XP_006723380.1:p.Phe4911Val
|
|
XM_006723319.2:c.14716T>G
|
XP_006723382.1:p.Phe4906Val
|
|
XM_011527205.2:c.14662T>G
|
XP_011525507.1:p.Phe4888Val
|
|
NM_000540.3:c.14749T>G
MANE Select
|
NP_000531.2:p.Phe4917Val
|
|
NM_001042723.2:c.14734T>G
|
NP_001036188.1:p.Phe4912Val
|
|