ENST00000344537.10:c.354G>C
MANE Select
|
ENSP00000341680.6:p.Leu118=
|
|
ENST00000338950.9:c.354G>C
|
ENSP00000344718.5:p.Leu118=
|
|
ENST00000344537.9:c.354G>C
|
ENSP00000341680.5:p.Leu118=
|
|
ENST00000355917.7:c.303G>C
|
ENSP00000348183.4:p.Leu101=
|
|
ENST00000506844.1:c.*352G>C
|
ENSP00000424202.1:n.*352G>C
|
|
ENST00000510395.5:c.*264G>C
|
ENSP00000424685.1:n.*264G>C
|
|
ENST00000511762.2:c.249G>C
|
ENSP00000427473.2:p.Leu83=
|
|
ENST00000513680.5:c.*352G>C
|
ENSP00000424357.1:n.*352G>C
|
|
ENST00000515875.5:c.303G>C
|
ENSP00000425495.1:p.Leu101=
|
|
ENST00000622898.4:c.249G>C
|
ENSP00000481997.1:p.Leu83=
|
|
NM_001271667.1:c.111G>C
|
NP_001258596.1:p.Leu37=
|
|
NM_001271668.1:c.303G>C
|
NP_001258597.1:p.Leu101=
|
|
NM_001271669.1:c.249G>C
|
NP_001258598.1:p.Leu83=
|
|
NM_032122.4:c.354G>C , LRG_588t1:c.354G>C
|
NP_115498.2:p.Leu118=
|
|
NM_183040.2:c.354G>C , LRG_588t2:c.354G>C
|
NP_898861.1:p.Leu118=
|
|
NR_036448.1:n.682G>C
|
|
|
XM_005249447.3:c.315G>C
|
XP_005249504.1:p.Leu105=
|
|
XM_011514936.1:c.264G>C
|
XP_011513238.1:p.Leu88=
|
|
XM_005249447.4:c.315G>C
|
XP_005249504.1:p.Leu105=
|
|
XM_011514936.3:c.264G>C
|
XP_011513238.1:p.Leu88=
|
|
NM_032122.5:c.354G>C
MANE Select
|
NP_115498.2:p.Leu118=
|
|
NR_036448.2:n.652G>C
|
|
|
NM_001271667.2:c.111G>C
|
NP_001258596.1:p.Leu37=
|
|
NM_001271668.2:c.303G>C
|
NP_001258597.1:p.Leu101=
|
|
NM_001271669.2:c.249G>C
|
NP_001258598.1:p.Leu83=
|
|
NR_036448.3:n.652G>C
|
|
|