ENST00000367049.9:c.4990G>T
MANE Select
|
ENSP00000356016.4:p.Asp1664Tyr
|
|
ENST00000367051.6:c.3640G>T
|
ENSP00000356018.1:p.Asp1214Tyr
|
|
ENST00000367052.6:c.3640G>T
|
ENSP00000356019.1:p.Asp1214Tyr
|
|
ENST00000367053.6:c.3640G>T
|
ENSP00000356020.1:p.Asp1214Tyr
|
|
ENST00000400960.7:c.3640G>T
|
ENSP00000383744.2:p.Asp1214Tyr
|
|
ENST00000367049.8:c.4990G>T
|
ENSP00000356016.4:p.Asp1664Tyr
|
|
ENST00000367051.5:c.3640G>T
|
ENSP00000356018.1:p.Asp1214Tyr
|
|
ENST00000367052.5:c.3640G>T
|
ENSP00000356019.1:p.Asp1214Tyr
|
|
ENST00000367053.5:c.3640G>T
|
ENSP00000356020.1:p.Asp1214Tyr
|
|
ENST00000400960.6:c.3640G>T
|
ENSP00000383744.2:p.Asp1214Tyr
|
|
ENST00000529814.1:c.1179+14370G>T
|
|
|
ENST00000534202.5:c.*755G>T
|
ENSP00000436139.2:n.*755G>T
|
|
NM_000573.3:c.3640G>T
|
NP_000564.2:p.Asp1214Tyr
|
|
NM_000651.4:c.4990G>T
|
NP_000642.3:p.Asp1664Tyr
|
|
XM_006711166.2:c.5005G>T
|
XP_006711229.1:p.Asp1669Tyr
|
|
XM_011509205.1:c.5005G>T
|
XP_011507507.1:p.Asp1669Tyr
|
|
NM_000651.5:c.4990G>T
|
NP_000642.3:p.Asp1664Tyr
|
|
XM_024453287.1:c.3655G>T
|
XP_024309055.1:p.Asp1219Tyr
|
|
NM_000573.4:c.3640G>T
|
NP_000564.2:p.Asp1214Tyr
|
|
NM_000651.6:c.4990G>T
MANE Select
|
NP_000642.3:p.Asp1664Tyr
|
|