ENST00000374479.4:c.1127G>T
MANE Select
|
ENSP00000363603.3:p.Arg376Leu
|
|
ENST00000374479.3:c.1127G>T
|
ENSP00000363603.3:p.Arg376Leu
|
|
NM_000147.4:c.1127G>T
|
NP_000138.2:p.Arg376Leu
|
|
XM_005245821.1:c.752G>T
|
XP_005245878.1:p.Arg251Leu
|
|
XM_011541167.1:c.494G>T
|
XP_011539469.1:p.Arg165Leu
|
|
XM_005245821.3:c.752G>T
|
XP_005245878.1:p.Arg251Leu
|
|
XM_011541167.3:c.494G>T
|
XP_011539469.1:p.Arg165Leu
|
|
XM_017000905.2:c.824G>T
|
XP_016856394.1:p.Arg275Leu
|
|
NM_000147.5:c.1127G>T
MANE Select
|
NP_000138.2:p.Arg376Leu
|
|
NR_174379.1:n.1305G>T
|
|
|
NR_174380.1:n.1354G>T
|
|
|
NR_174381.1:n.1193G>T
|
|
|
NR_174382.1:n.1590G>T
|
|
|