|
ENST00000344537.10:c.176G>A
MANE Select
|
ENSP00000341680.6:p.Trp59Ter
|
|
|
ENST00000338950.9:c.176G>A
|
ENSP00000344718.5:p.Trp59Ter
|
|
|
ENST00000344537.9:c.176G>A
|
ENSP00000341680.5:p.Trp59Ter
|
|
|
ENST00000355917.7:c.125G>A
|
ENSP00000348183.4:p.Trp42Ter
|
|
|
ENST00000506844.1:c.*174G>A
|
ENSP00000424202.1:n.*174G>A
|
|
|
ENST00000510395.5:c.*86G>A
|
ENSP00000424685.1:n.*86G>A
|
|
|
ENST00000511762.2:c.71G>A
|
ENSP00000427473.2:p.Trp24Ter
|
|
|
ENST00000513680.5:c.*174G>A
|
ENSP00000424357.1:n.*174G>A
|
|
|
ENST00000515875.5:c.125G>A
|
ENSP00000425495.1:p.Trp42Ter
|
|
|
ENST00000622898.4:c.71G>A
|
ENSP00000481997.1:p.Trp24Ter
|
|
|
NM_001271667.1:c.-68G>A
|
NP_001258596.1:n.-68G>A
|
|
|
NM_001271668.1:c.125G>A
|
NP_001258597.1:p.Trp42Ter
|
|
|
NM_001271669.1:c.71G>A
|
NP_001258598.1:p.Trp24Ter
|
|
|
NM_032122.4:c.176G>A , LRG_588t1:c.176G>A
|
NP_115498.2:p.Trp59Ter
|
|
|
NM_183040.2:c.176G>A , LRG_588t2:c.176G>A
|
NP_898861.1:p.Trp59Ter
|
|
|
NR_036448.1:n.504G>A
|
|
|
|
XM_005249447.3:c.137G>A
|
XP_005249504.1:p.Trp46Ter
|
|
|
XM_011514936.1:c.86G>A
|
XP_011513238.1:p.Trp29Ter
|
|
|
XM_005249447.4:c.137G>A
|
XP_005249504.1:p.Trp46Ter
|
|
|
XM_011514936.3:c.86G>A
|
XP_011513238.1:p.Trp29Ter
|
|
|
NM_032122.5:c.176G>A
MANE Select
|
NP_115498.2:p.Trp59Ter
|
|
|
NR_036448.2:n.474G>A
|
|
|
|
NM_001271667.2:c.-68G>A
|
NP_001258596.1:n.-68G>A
|
|
|
NM_001271668.2:c.125G>A
|
NP_001258597.1:p.Trp42Ter
|
|
|
NM_001271669.2:c.71G>A
|
NP_001258598.1:p.Trp24Ter
|
|
|
NR_036448.3:n.474G>A
|
|
|
