ENST00000684241.1:n.3977G>T
|
|
|
ENST00000262186.10:c.3144G>T
MANE Select
|
ENSP00000262186.5:p.Gln1048His
|
|
ENST00000330883.9:c.2124G>T
|
ENSP00000328531.4:p.Gln708His
|
|
ENST00000262186.9:c.3144G>T
|
ENSP00000262186.5:p.Gln1048His
|
|
ENST00000330883.8:c.2124G>T
|
ENSP00000328531.4:p.Gln708His
|
|
NM_000238.3:c.3144G>T , LRG_288t1:c.3144G>T
|
NP_000229.1:p.Gln1048His
|
|
NM_172057.2:c.2124G>T , LRG_288t3:c.2124G>T
|
NP_742054.1:p.Gln708His
|
|
XM_011516185.1:c.2844G>T
|
XP_011514487.1:p.Gln948His
|
|
XM_011516185.2:c.2844G>T
|
XP_011514487.1:p.Gln948His
|
|
XM_017012195.1:c.2994G>T
|
XP_016867684.1:p.Gln998His
|
|
XM_017012196.1:c.2967G>T
|
XP_016867685.1:p.Gln989His
|
|
NM_000238.4:c.3144G>T
MANE Select
|
NP_000229.1:p.Gln1048His
|
|
NM_172057.3:c.2124G>T
|
NP_742054.1:p.Gln708His
|
|