ENST00000344537.10:c.331T>G
MANE Select
|
ENSP00000341680.6:p.Leu111Val
|
|
ENST00000338950.9:c.331T>G
|
ENSP00000344718.5:p.Leu111Val
|
|
ENST00000344537.9:c.331T>G
|
ENSP00000341680.5:p.Leu111Val
|
|
ENST00000355917.7:c.280T>G
|
ENSP00000348183.4:p.Leu94Val
|
|
ENST00000506844.1:c.*329T>G
|
ENSP00000424202.1:n.*329T>G
|
|
ENST00000510395.5:c.*241T>G
|
ENSP00000424685.1:n.*241T>G
|
|
ENST00000511762.2:c.226T>G
|
ENSP00000427473.2:p.Leu76Val
|
|
ENST00000513680.5:c.*329T>G
|
ENSP00000424357.1:n.*329T>G
|
|
ENST00000515875.5:c.280T>G
|
ENSP00000425495.1:p.Leu94Val
|
|
ENST00000622898.4:c.226T>G
|
ENSP00000481997.1:p.Leu76Val
|
|
NM_001271667.1:c.88T>G
|
NP_001258596.1:p.Leu30Val
|
|
NM_001271668.1:c.280T>G
|
NP_001258597.1:p.Leu94Val
|
|
NM_001271669.1:c.226T>G
|
NP_001258598.1:p.Leu76Val
|
|
NM_032122.4:c.331T>G , LRG_588t1:c.331T>G
|
NP_115498.2:p.Leu111Val
|
|
NM_183040.2:c.331T>G , LRG_588t2:c.331T>G
|
NP_898861.1:p.Leu111Val
|
|
NR_036448.1:n.659T>G
|
|
|
XM_005249447.3:c.292T>G
|
XP_005249504.1:p.Leu98Val
|
|
XM_011514936.1:c.241T>G
|
XP_011513238.1:p.Leu81Val
|
|
XM_005249447.4:c.292T>G
|
XP_005249504.1:p.Leu98Val
|
|
XM_011514936.3:c.241T>G
|
XP_011513238.1:p.Leu81Val
|
|
NM_032122.5:c.331T>G
MANE Select
|
NP_115498.2:p.Leu111Val
|
|
NR_036448.2:n.629T>G
|
|
|
NM_001271667.2:c.88T>G
|
NP_001258596.1:p.Leu30Val
|
|
NM_001271668.2:c.280T>G
|
NP_001258597.1:p.Leu94Val
|
|
NM_001271669.2:c.226T>G
|
NP_001258598.1:p.Leu76Val
|
|
NR_036448.3:n.629T>G
|
|
|