ENST00000334785.12:c.1146A>C
MANE Select
|
ENSP00000333938.7:p.Leu382Phe
|
|
ENST00000330010.12:c.954A>C
|
ENSP00000327363.8:p.Leu318Phe
|
|
ENST00000334785.11:c.1146A>C
|
ENSP00000333938.7:p.Leu382Phe
|
|
ENST00000342754.5:c.845A>C
|
|
|
ENST00000401035.7:c.954A>C
|
ENSP00000383814.3:p.Leu318Phe
|
|
ENST00000440324.5:c.1104A>C
|
ENSP00000411902.1:p.Leu368Phe
|
|
ENST00000464998.1:n.606A>C
|
|
|
ENST00000480732.2:n.720A>C
|
|
|
NM_001172309.1:c.954A>C
|
NP_001165780.1:p.Leu318Phe
|
|
NM_144573.3:c.1146A>C , LRG_442t1:c.1146A>C
|
NP_653174.3:p.Leu382Phe
|
|
XM_005271322.2:c.1146A>C
|
XP_005271379.1:p.Leu382Phe
|
|
XM_005271323.2:c.1104A>C
|
XP_005271380.1:p.Leu368Phe
|
|
XM_005271324.3:c.954A>C
|
XP_005271381.1:p.Leu318Phe
|
|
XM_005271325.2:c.1146A>C
|
XP_005271382.1:p.Leu382Phe
|
|
XM_005271326.2:c.912A>C
|
XP_005271383.1:p.Leu304Phe
|
|
XM_005271327.2:c.729A>C
|
XP_005271384.1:p.Leu243Phe
|
|
XM_005271322.4:c.1146A>C
|
XP_005271379.1:p.Leu382Phe
|
|
XM_005271323.4:c.1104A>C
|
XP_005271380.1:p.Leu368Phe
|
|
XM_005271324.5:c.954A>C
|
XP_005271381.1:p.Leu318Phe
|
|
XM_005271325.4:c.1146A>C
|
XP_005271382.1:p.Leu382Phe
|
|
XM_005271326.4:c.912A>C
|
XP_005271383.1:p.Leu304Phe
|
|
XM_005271327.4:c.729A>C
|
XP_005271384.1:p.Leu243Phe
|
|
NM_001172309.2:c.954A>C
|
NP_001165780.1:p.Leu318Phe
|
|
NM_144573.4:c.1146A>C
MANE Select
|
NP_653174.3:p.Leu382Phe
|
|