ENST00000682089.1:n.541A>C
|
|
|
ENST00000682266.1:c.771A>C
|
ENSP00000507766.1:p.Arg257Ser
|
|
ENST00000682341.1:c.1179A>C
|
ENSP00000508251.1:p.Arg393Ser
|
|
ENST00000682530.1:c.*1153A>C
|
ENSP00000506805.1:n.*1153A>C
|
|
ENST00000683197.1:c.1179A>C
|
ENSP00000507641.1:p.Arg393Ser
|
|
ENST00000683411.1:c.771A>C
|
ENSP00000508397.1:p.Arg257Ser
|
|
ENST00000683437.1:c.771A>C
|
ENSP00000508408.1:p.Arg257Ser
|
|
ENST00000683613.1:n.2215A>C
|
|
|
ENST00000683834.1:n.1421A>C
|
|
|
ENST00000684663.1:c.1176A>C
|
ENSP00000508009.1:p.Arg392Ser
|
|
ENST00000324559.9:c.1221A>C
MANE Select
|
ENSP00000315371.9:p.Arg407Ser
|
|
ENST00000648804.1:n.1556A>C
|
|
|
ENST00000324559.8:c.1221A>C
|
ENSP00000315371.8:p.Arg407Ser
|
|
NM_001142649.1:c.1218A>C
|
NP_001136121.1:p.Arg406Ser
|
|
NM_213599.2:c.1221A>C , LRG_868t1:c.1221A>C
|
NP_998764.1:p.Arg407Ser
|
|
XM_005252820.2:c.1179A>C
|
XP_005252877.2:p.Arg393Ser
|
|
XM_005252821.2:c.1176A>C
|
XP_005252878.2:p.Arg392Ser
|
|
XM_005252822.3:c.1143A>C
|
XP_005252879.1:p.Arg381Ser
|
|
XM_005252823.3:c.1140A>C
|
XP_005252880.1:p.Arg380Ser
|
|
XM_011519949.1:c.1128A>C
|
XP_011518251.1:p.Arg376Ser
|
|
XM_005252820.3:c.1179A>C
|
XP_005252877.2:p.Arg393Ser
|
|
XM_005252821.3:c.1176A>C
|
XP_005252878.2:p.Arg392Ser
|
|
XM_005252822.4:c.1143A>C
|
XP_005252879.1:p.Arg381Ser
|
|
XM_011519949.2:c.1128A>C
|
XP_011518251.1:p.Arg376Ser
|
|
NM_001142649.2:c.1218A>C
|
NP_001136121.1:p.Arg406Ser
|
|
NM_213599.3:c.1221A>C
MANE Select
|
NP_998764.1:p.Arg407Ser
|
|