ENST00000682089.1:n.306T>C
|
|
|
ENST00000682266.1:c.536T>C
|
ENSP00000507766.1:p.Leu179Ser
|
|
ENST00000682341.1:c.944T>C
|
ENSP00000508251.1:p.Leu315Ser
|
|
ENST00000682530.1:c.*918T>C
|
ENSP00000506805.1:n.*918T>C
|
|
ENST00000683197.1:c.944T>C
|
ENSP00000507641.1:p.Leu315Ser
|
|
ENST00000683411.1:c.536T>C
|
ENSP00000508397.1:p.Leu179Ser
|
|
ENST00000683437.1:c.536T>C
|
ENSP00000508408.1:p.Leu179Ser
|
|
ENST00000683613.1:n.1980T>C
|
|
|
ENST00000683834.1:n.1186T>C
|
|
|
ENST00000684663.1:c.941T>C
|
ENSP00000508009.1:p.Leu314Ser
|
|
ENST00000324559.9:c.986T>C
MANE Select
|
ENSP00000315371.9:p.Leu329Ser
|
|
ENST00000648804.1:n.1321T>C
|
|
|
ENST00000324559.8:c.986T>C
|
ENSP00000315371.8:p.Leu329Ser
|
|
NM_001142649.1:c.983T>C
|
NP_001136121.1:p.Leu328Ser
|
|
NM_213599.2:c.986T>C , LRG_868t1:c.986T>C
|
NP_998764.1:p.Leu329Ser
|
|
XM_005252820.2:c.944T>C
|
XP_005252877.2:p.Leu315Ser
|
|
XM_005252821.2:c.941T>C
|
XP_005252878.2:p.Leu314Ser
|
|
XM_005252822.3:c.908T>C
|
XP_005252879.1:p.Leu303Ser
|
|
XM_005252823.3:c.905T>C
|
XP_005252880.1:p.Leu302Ser
|
|
XM_011519949.1:c.893T>C
|
XP_011518251.1:p.Leu298Ser
|
|
XM_005252820.3:c.944T>C
|
XP_005252877.2:p.Leu315Ser
|
|
XM_005252821.3:c.941T>C
|
XP_005252878.2:p.Leu314Ser
|
|
XM_005252822.4:c.908T>C
|
XP_005252879.1:p.Leu303Ser
|
|
XM_011519949.2:c.893T>C
|
XP_011518251.1:p.Leu298Ser
|
|
NM_001142649.2:c.983T>C
|
NP_001136121.1:p.Leu328Ser
|
|
NM_213599.3:c.986T>C
MANE Select
|
NP_998764.1:p.Leu329Ser
|
|