ENST00000684241.1:n.3335T>G
|
|
|
ENST00000262186.10:c.2502T>G
MANE Select
|
ENSP00000262186.5:p.His834Gln
|
|
ENST00000330883.9:c.1482T>G
|
ENSP00000328531.4:p.His494Gln
|
|
ENST00000262186.9:c.2502T>G
|
ENSP00000262186.5:p.His834Gln
|
|
ENST00000330883.8:c.1482T>G
|
ENSP00000328531.4:p.His494Gln
|
|
NM_000238.3:c.2502T>G , LRG_288t1:c.2502T>G
|
NP_000229.1:p.His834Gln
|
|
NM_172057.2:c.1482T>G , LRG_288t3:c.1482T>G
|
NP_742054.1:p.His494Gln
|
|
XM_011516185.1:c.2202T>G
|
XP_011514487.1:p.His734Gln
|
|
XM_011516186.1:c.2502T>G
|
XP_011514488.1:p.His834Gln
|
|
XM_011516185.2:c.2202T>G
|
XP_011514487.1:p.His734Gln
|
|
XM_011516186.3:c.2502T>G
|
XP_011514488.1:p.His834Gln
|
|
XM_017012195.1:c.2352T>G
|
XP_016867684.1:p.His784Gln
|
|
XM_017012196.1:c.2325T>G
|
XP_016867685.1:p.His775Gln
|
|
NM_000238.4:c.2502T>G
MANE Select
|
NP_000229.1:p.His834Gln
|
|
NM_172057.3:c.1482T>G
|
NP_742054.1:p.His494Gln
|
|