|
NM_006424.3:c.1242G>T
MANE Select
|
NP_006415.3:p.Leu414Phe
|
|
ENST00000382051.8:c.1242G>T
MANE Select
|
ENSP00000371483.3:p.Leu414Phe
|
|
NM_001177998.1:c.1239G>T
|
NP_001171469.1:p.Leu413Phe
|
|
NM_001177998.2:c.1239G>T
|
NP_001171469.2:p.Leu413Phe
|
|
NM_001177999.1:c.1239G>T
|
NP_001171470.1:p.Leu413Phe
|
|
NM_001177999.2:c.1239G>T
|
NP_001171470.2:p.Leu413Phe
|
|
NM_006424.2:c.1242G>T
|
NP_006415.2:p.Leu414Phe
|
|
ENST00000382051.7:c.1242G>T
|
ENSP00000371483.3:p.Leu414Phe
|
|
ENST00000503434.5:c.1239G>T
|
ENSP00000423021.1:p.Leu413Phe
|
|
ENST00000504570.5:c.1239G>T
|
ENSP00000425501.1:p.Leu413Phe
|
|
ENST00000645788.1:c.1239G>T
|
ENSP00000494094.1:p.Leu413Phe
|