ENST00000261769.10:c.2419A>T
MANE Select
|
ENSP00000261769.4:p.Ile807Phe
|
|
ENST00000261769.9:c.2419A>T
|
ENSP00000261769.4:p.Ile807Phe
|
|
ENST00000422392.6:c.2236A>T
|
ENSP00000414946.2:p.Ile746Phe
|
|
ENST00000562118.1:n.637A>T
|
|
|
ENST00000562836.5:n.2490A>T
|
|
|
ENST00000566510.5:c.*1085A>T
|
ENSP00000458139.1:n.*1085A>T
|
|
ENST00000566612.5:c.*659A>T
|
ENSP00000454782.1:n.*659A>T
|
|
ENST00000611625.4:c.2482A>T
|
ENSP00000481063.1:p.Ile828Phe
|
|
ENST00000612417.4:c.1853+3223A>T
|
ENSP00000478360.1:n.1853+3223A>T
|
|
ENST00000621016.4:c.1866-4426A>T
|
ENSP00000480664.1:n.1866-4426A>T
|
|
NM_004360.3:c.2419A>T , LRG_301t1:c.2419A>T
|
NP_004351.1:p.Ile807Phe
|
|
XM_011523488.1:c.1684A>T
|
XP_011521790.1:p.Ile562Phe
|
|
XM_011523489.1:c.1684A>T
|
XP_011521791.1:p.Ile562Phe
|
|
NM_001317184.1:c.2236A>T
|
NP_001304113.1:p.Ile746Phe
|
|
NM_001317185.1:c.871A>T
|
NP_001304114.1:p.Ile291Phe
|
|
NM_001317186.1:c.454A>T
|
NP_001304115.1:p.Ile152Phe
|
|
NM_004360.4:c.2419A>T
|
NP_004351.1:p.Ile807Phe
|
|
NM_004360.5:c.2419A>T
MANE Select
|
NP_004351.1:p.Ile807Phe
|
|
NM_001317184.2:c.2236A>T
|
NP_001304113.1:p.Ile746Phe
|
|
NM_001317185.2:c.871A>T
|
NP_001304114.1:p.Ile291Phe
|
|
NM_001317186.2:c.454A>T
|
NP_001304115.1:p.Ile152Phe
|
|