ENST00000356392.9:c.1257G>T
MANE Select
|
ENSP00000348757.3:p.Ser419=
|
|
ENST00000356392.8:c.1257G>T
|
ENSP00000348757.3:p.Ser419=
|
|
ENST00000586836.5:c.684G>T
|
ENSP00000467429.1:p.Ser228=
|
|
ENST00000591179.5:c.1077G>T
|
ENSP00000466800.1:p.Ser359=
|
|
ENST00000591345.5:c.*1176G>T
|
ENSP00000467313.1:n.*1176G>T
|
|
NM_001302453.1:c.1095G>T
|
NP_001289382.1:p.Ser365=
|
|
NM_001302454.1:c.1077G>T
|
NP_001289383.1:p.Ser359=
|
|
NM_145045.4:c.1257G>T
|
NP_659482.3:p.Ser419=
|
|
NM_145045.5:c.1257G>T
MANE Select
|
NP_659482.3:p.Ser419=
|
|
NM_001302454.2:c.1077G>T
|
NP_001289383.1:p.Ser359=
|
|