ENST00000330889.8:c.1092G>T
MANE Select
|
ENSP00000329468.3:p.Leu364Phe
|
|
ENST00000330889.7:c.1092G>T
|
ENSP00000329468.3:p.Leu364Phe
|
|
ENST00000470962.1:n.512G>T
|
|
|
ENST00000480980.1:n.526G>T
|
|
|
ENST00000580525.5:c.1110G>T
|
ENSP00000464121.1:p.Leu370Phe
|
|
ENST00000584828.5:c.402+59G>T
|
|
|
ENST00000585130.5:c.*691G>T
|
ENSP00000464120.1:n.*691G>T
|
|
NM_018404.2:c.1092G>T
|
NP_060874.1:p.Leu364Phe
|
|
XM_005258008.2:c.1110G>T
|
XP_005258065.1:p.Leu370Phe
|
|
XM_005258011.2:c.1047G>T
|
XP_005258068.1:p.Leu349Phe
|
|
XM_006721973.2:c.1051+59G>T
|
XP_006722036.1:n.1051+59G>T
|
|
XM_011524993.1:c.1107G>T
|
XP_011523295.1:p.Leu369Phe
|
|
XM_011524994.1:c.1089G>T
|
XP_011523296.1:p.Leu363Phe
|
|
NM_001346712.1:c.1110G>T
|
NP_001333641.1:p.Leu370Phe
|
|
NM_001346714.1:c.1089G>T
|
NP_001333643.1:p.Leu363Phe
|
|
NM_001346716.1:c.1033+59G>T
|
NP_001333645.1:n.1033+59G>T
|
|
NR_144488.1:n.1291G>T
|
|
|
XM_024450831.1:c.1092G>T
|
XP_024306599.1:p.Leu364Phe
|
|
XM_024450832.1:c.1107G>T
|
XP_024306600.1:p.Leu369Phe
|
|
XM_024450833.1:c.1047G>T
|
XP_024306601.1:p.Leu349Phe
|
|
XM_024450834.1:c.1051+59G>T
|
XP_024306602.1:n.1051+59G>T
|
|
XM_024450835.1:c.726G>T
|
XP_024306603.1:p.Leu242Phe
|
|
NM_018404.3:c.1092G>T
MANE Select
|
NP_060874.1:p.Leu364Phe
|
|
NM_001346712.2:c.1110G>T
|
NP_001333641.1:p.Leu370Phe
|
|
NM_001346714.2:c.1089G>T
|
NP_001333643.1:p.Leu363Phe
|
|
NM_001346716.2:c.1033+59G>T
|
NP_001333645.1:n.1033+59G>T
|
|
NR_144488.2:n.1082G>T
|
|
|