ENST00000461280.2:n.1604T>G
|
|
|
ENST00000684241.1:n.3139T>G
|
|
|
ENST00000262186.10:c.2306T>G
MANE Select
|
ENSP00000262186.5:p.Leu769Arg
|
|
ENST00000330883.9:c.1286T>G
|
ENSP00000328531.4:p.Leu429Arg
|
|
ENST00000262186.9:c.2306T>G
|
ENSP00000262186.5:p.Leu769Arg
|
|
ENST00000330883.8:c.1286T>G
|
ENSP00000328531.4:p.Leu429Arg
|
|
ENST00000430723.4:c.1958T>G
|
ENSP00000387657.4:p.Leu653Arg
|
|
ENST00000461280.1:n.1593T>G
|
|
|
ENST00000473610.5:n.1938T>G
|
|
|
ENST00000532957.5:n.2529T>G
|
|
|
NM_000238.3:c.2306T>G , LRG_288t1:c.2306T>G
|
NP_000229.1:p.Leu769Arg
|
|
NM_001204798.1:c.1286T>G
|
NP_001191727.1:p.Leu429Arg
|
|
NM_172056.2:c.2306T>G , LRG_288t2:c.2306T>G
|
NP_742053.1:p.Leu769Arg
|
|
NM_172057.2:c.1286T>G , LRG_288t3:c.1286T>G
|
NP_742054.1:p.Leu429Arg
|
|
XM_011516185.1:c.2006T>G
|
XP_011514487.1:p.Leu669Arg
|
|
XM_011516186.1:c.2306T>G
|
XP_011514488.1:p.Leu769Arg
|
|
XM_011516185.2:c.2006T>G
|
XP_011514487.1:p.Leu669Arg
|
|
XM_011516186.3:c.2306T>G
|
XP_011514488.1:p.Leu769Arg
|
|
XM_017012195.1:c.2156T>G
|
XP_016867684.1:p.Leu719Arg
|
|
XM_017012196.1:c.2129T>G
|
XP_016867685.1:p.Leu710Arg
|
|
NM_000238.4:c.2306T>G
MANE Select
|
NP_000229.1:p.Leu769Arg
|
|
NM_001204798.2:c.1286T>G
|
NP_001191727.1:p.Leu429Arg
|
|
NM_172057.3:c.1286T>G
|
NP_742054.1:p.Leu429Arg
|
|