ENST00000356392.9:c.1332G>T
MANE Select
|
ENSP00000348757.3:p.Arg444=
|
|
ENST00000356392.8:c.1332G>T
|
ENSP00000348757.3:p.Arg444=
|
|
ENST00000586836.5:c.759G>T
|
ENSP00000467429.1:p.Arg253=
|
|
ENST00000591179.5:c.1152G>T
|
ENSP00000466800.1:p.Arg384=
|
|
ENST00000591345.5:c.*1251G>T
|
ENSP00000467313.1:n.*1251G>T
|
|
NM_001302453.1:c.1170G>T
|
NP_001289382.1:p.Arg390=
|
|
NM_001302454.1:c.1152G>T
|
NP_001289383.1:p.Arg384=
|
|
NM_145045.4:c.1332G>T
|
NP_659482.3:p.Arg444=
|
|
NM_145045.5:c.1332G>T
MANE Select
|
NP_659482.3:p.Arg444=
|
|
NM_001302454.2:c.1152G>T
|
NP_001289383.1:p.Arg384=
|
|