ENST00000338382.11:c.497T>C
MANE Select
|
ENSP00000344307.6:p.Leu166Ser
|
|
ENST00000338382.10:c.497T>C
|
ENSP00000344307.6:p.Leu166Ser
|
|
ENST00000380249.5:c.497T>C
|
ENSP00000369599.1:p.Leu166Ser
|
|
ENST00000604103.1:n.290-3T>C
|
|
|
ENST00000605031.5:n.273T>C
|
|
|
NM_017794.4:c.497T>C
|
NP_060264.4:p.Leu166Ser
|
|
XM_005251494.3:c.497T>C
|
XP_005251551.2:p.Leu166Ser
|
|
XM_011517944.1:c.497T>C
|
XP_011516246.1:p.Leu166Ser
|
|
XM_011517945.1:c.392T>C
|
XP_011516247.1:p.Leu131Ser
|
|
XM_011517946.1:c.497T>C
|
XP_011516248.1:p.Leu166Ser
|
|
XM_011517947.1:c.497T>C
|
XP_011516249.1:p.Leu166Ser
|
|
XM_011517948.1:c.497T>C
|
XP_011516250.1:p.Leu166Ser
|
|
XM_005251494.4:c.497T>C
|
XP_005251551.2:p.Leu166Ser
|
|
XM_011517945.2:c.392T>C
|
XP_011516247.1:p.Leu131Ser
|
|
XM_017014852.1:c.578T>C
|
XP_016870341.1:p.Leu193Ser
|
|
XM_017014853.1:c.578T>C
|
XP_016870342.1:p.Leu193Ser
|
|
XM_017014854.1:c.473T>C
|
XP_016870343.1:p.Leu158Ser
|
|
XM_017014855.1:c.578T>C
|
XP_016870344.1:p.Leu193Ser
|
|
XM_017014856.1:c.578T>C
|
XP_016870345.1:p.Leu193Ser
|
|
XM_017014857.2:c.497T>C
|
XP_016870346.1:p.Leu166Ser
|
|
XM_017014858.2:c.392T>C
|
XP_016870347.1:p.Leu131Ser
|
|
XM_017014859.1:c.-23T>C
|
XP_016870348.1:n.-23T>C
|
|
XM_024447585.1:c.497T>C
|
XP_024303353.1:p.Leu166Ser
|
|
XM_024447586.1:c.182T>C
|
XP_024303354.1:p.Leu61Ser
|
|
NM_001375567.1:c.497T>C
MANE Select
|
NP_001362496.1:p.Leu166Ser
|
|
NM_001375568.1:c.497T>C
|
NP_001362497.1:p.Leu166Ser
|
|
NM_001375570.1:c.392T>C
|
NP_001362499.1:p.Leu131Ser
|
|
NM_017794.5:c.497T>C
|
NP_060264.4:p.Leu166Ser
|
|