ENST00000373327.5:c.1838C>T
MANE Select
|
ENSP00000362424.4:p.Ala613Val
|
|
ENST00000373327.4:c.1838C>T
|
ENSP00000362424.4:p.Ala613Val
|
|
ENST00000391993.7:c.1640C>T
|
ENSP00000375851.3:p.Ala547Val
|
|
ENST00000462122.1:n.849C>T
|
|
|
ENST00000483951.1:n.186C>T
|
|
|
NM_001139490.1:c.1640C>T
|
NP_001132962.1:p.Ala547Val
|
|
NM_015650.3:c.1838C>T
|
NP_056465.2:p.Ala613Val
|
|
XM_006712414.1:c.1637C>T
|
XP_006712477.1:p.Ala546Val
|
|
XM_011510944.1:c.1940C>T
|
XP_011509246.1:p.Ala647Val
|
|
XM_011510945.1:c.1901C>T
|
XP_011509247.1:p.Ala634Val
|
|
XM_011510946.1:c.1868C>T
|
XP_011509248.1:p.Ala623Val
|
|
XM_011510947.1:c.1808C>T
|
XP_011509249.1:p.Ala603Val
|
|
XM_011510948.1:c.1742C>T
|
XP_011509250.1:p.Ala581Val
|
|
XM_011510950.1:c.806C>T
|
XP_011509252.1:p.Ala269Val
|
|
XM_006712414.2:c.1637C>T
|
XP_006712477.1:p.Ala546Val
|
|
XM_011510944.2:c.1940C>T
|
XP_011509246.1:p.Ala647Val
|
|
XM_011510945.2:c.1901C>T
|
XP_011509247.1:p.Ala634Val
|
|
XM_011510946.2:c.1868C>T
|
XP_011509248.1:p.Ala623Val
|
|
XM_011510947.2:c.1808C>T
|
XP_011509249.1:p.Ala603Val
|
|
XM_011510948.2:c.1742C>T
|
XP_011509250.1:p.Ala581Val
|
|
XM_011510950.2:c.806C>T
|
XP_011509252.1:p.Ala269Val
|
|
XM_017003789.1:c.1937C>T
|
XP_016859278.1:p.Ala646Val
|
|
XR_001738696.1:n.1666C>T
|
|
|
XR_001738697.1:n.1663C>T
|
|
|
NM_015650.4:c.1838C>T
MANE Select
|
NP_056465.2:p.Ala613Val
|
|