ENST00000684241.1:n.1588_1601del
|
|
|
ENST00000262186.10:c.755_768del
MANE Select
|
ENSP00000262186.5:p.Arg252GlnfsTer?
|
|
ENST00000262186.9:c.755_768del
|
ENSP00000262186.5:p.Arg252GlnfsTer?
|
|
ENST00000430723.4:c.407_420del
|
ENSP00000387657.4:p.Arg136GlnfsTer?
|
|
ENST00000532957.5:n.978_991del
|
|
|
NM_000238.3:c.755_768del , LRG_288t1:c.755_768del
|
NP_000229.1:p.Arg252GlnfsTer?
|
|
NM_172056.2:c.755_768del , LRG_288t2:c.755_768del
|
NP_742053.1:p.Arg252GlnfsTer?
|
|
XM_011516185.1:c.455_468del
|
XP_011514487.1:p.Arg152GlnfsTer?
|
|
XM_011516186.1:c.755_768del
|
XP_011514488.1:p.Arg252GlnfsTer?
|
|
XM_011516185.2:c.455_468del
|
XP_011514487.1:p.Arg152GlnfsTer?
|
|
XM_011516186.3:c.755_768del
|
XP_011514488.1:p.Arg252GlnfsTer?
|
|
XM_017012195.1:c.605_618del
|
XP_016867684.1:p.Arg202GlnfsTer?
|
|
XM_017012196.1:c.578_591del
|
XP_016867685.1:p.Arg193GlnfsTer?
|
|
NM_000238.4:c.755_768del
MANE Select
|
NP_000229.1:p.Arg252GlnfsTer?
|
|