ENST00000373327.5:c.1906C>T
MANE Select
|
ENSP00000362424.4:p.Gln636Ter
|
|
ENST00000373327.4:c.1906C>T
|
ENSP00000362424.4:p.Gln636Ter
|
|
ENST00000391993.7:c.1708C>T
|
ENSP00000375851.3:p.Gln570Ter
|
|
ENST00000462122.1:n.917C>T
|
|
|
ENST00000483951.1:n.254C>T
|
|
|
NM_001139490.1:c.1708C>T
|
NP_001132962.1:p.Gln570Ter
|
|
NM_015650.3:c.1906C>T
|
NP_056465.2:p.Gln636Ter
|
|
XM_006712414.1:c.1705C>T
|
XP_006712477.1:p.Gln569Ter
|
|
XM_011510944.1:c.2008C>T
|
XP_011509246.1:p.Gln670Ter
|
|
XM_011510945.1:c.1969C>T
|
XP_011509247.1:p.Gln657Ter
|
|
XM_011510946.1:c.1936C>T
|
XP_011509248.1:p.Gln646Ter
|
|
XM_011510947.1:c.1876C>T
|
XP_011509249.1:p.Gln626Ter
|
|
XM_011510948.1:c.1810C>T
|
XP_011509250.1:p.Gln604Ter
|
|
XM_011510950.1:c.874C>T
|
XP_011509252.1:p.Gln292Ter
|
|
XM_006712414.2:c.1705C>T
|
XP_006712477.1:p.Gln569Ter
|
|
XM_011510944.2:c.2008C>T
|
XP_011509246.1:p.Gln670Ter
|
|
XM_011510945.2:c.1969C>T
|
XP_011509247.1:p.Gln657Ter
|
|
XM_011510946.2:c.1936C>T
|
XP_011509248.1:p.Gln646Ter
|
|
XM_011510947.2:c.1876C>T
|
XP_011509249.1:p.Gln626Ter
|
|
XM_011510948.2:c.1810C>T
|
XP_011509250.1:p.Gln604Ter
|
|
XM_011510950.2:c.874C>T
|
XP_011509252.1:p.Gln292Ter
|
|
XM_017003789.1:c.2005C>T
|
XP_016859278.1:p.Gln669Ter
|
|
XR_001738696.1:n.1734C>T
|
|
|
XR_001738697.1:n.1731C>T
|
|
|
NM_015650.4:c.1906C>T
MANE Select
|
NP_056465.2:p.Gln636Ter
|
|