|
ENST00000382329.2:c.2173C>T
|
ENSP00000371766.2:p.His725Tyr
|
|
|
ENST00000382331.6:n.874C>T
|
|
|
|
ENST00000483757.6:c.*1064C>T
|
ENSP00000417691.2:n.*1064C>T
|
|
|
ENST00000682260.1:n.2273C>T
|
|
|
|
ENST00000685949.1:n.1165C>T
|
|
|
|
ENST00000432829.7:c.2377C>T
MANE Select
|
ENSP00000394888.3:p.His793Tyr
|
|
|
ENST00000382329.1:c.778C>T
|
ENSP00000371766.1:p.His260Tyr
|
|
|
ENST00000382331.5:c.283C>T
|
ENSP00000371768.1:p.His95Tyr
|
|
|
ENST00000432829.6:c.2377C>T
|
ENSP00000394888.3:p.His793Tyr
|
|
|
ENST00000453981.5:c.2173C>T
|
ENSP00000408464.2:p.His725Tyr
|
|
|
ENST00000469391.5:c.2173C>T
|
ENSP00000419438.1:p.His725Tyr
|
|
|
ENST00000483757.5:c.*1852C>T
|
ENSP00000417691.1:n.*1852C>T
|
|
|
ENST00000495184.5:n.4332C>T
|
|
|
|
NM_001190458.1:c.2173C>T
|
NP_001177387.1:p.His725Tyr
|
|
|
NM_001193536.1:c.2173C>T
|
NP_001180465.1:p.His725Tyr
|
|
|
NM_203447.3:c.2377C>T , LRG_196t1:c.2377C>T
|
NP_982272.2:p.His793Tyr
|
|
|
XM_011518045.1:c.2173C>T
|
XP_011516347.1:p.His725Tyr
|
|
|
XM_011518046.1:c.2239C>T
|
XP_011516348.1:p.His747Tyr
|
|
|
XM_011518047.1:c.2173C>T
|
XP_011516349.1:p.His725Tyr
|
|
|
XM_011518048.1:c.2173C>T
|
XP_011516350.1:p.His725Tyr
|
|
|
XM_011518049.1:c.613C>T
|
XP_011516351.1:p.His205Tyr
|
|
|
XM_011518045.3:c.2173C>T
|
XP_011516347.1:p.His725Tyr
|
|
|
XM_011518046.2:c.2239C>T
|
XP_011516348.1:p.His747Tyr
|
|
|
XM_011518047.3:c.2173C>T
|
XP_011516349.1:p.His725Tyr
|
|
|
XM_011518048.2:c.2173C>T
|
XP_011516350.1:p.His725Tyr
|
|
|
XM_011518049.2:c.613C>T
|
XP_011516351.1:p.His205Tyr
|
|
|
XM_017015173.1:c.2173C>T
|
XP_016870662.1:p.His725Tyr
|
|
|
XM_017015174.1:c.2239C>T
|
XP_016870663.1:p.His747Tyr
|
|
|
NM_001190458.2:c.2173C>T
|
NP_001177387.1:p.His725Tyr
|
|
|
NM_001193536.2:c.2173C>T
|
NP_001180465.1:p.His725Tyr
|
|
|
NM_203447.4:c.2377C>T
MANE Select
|
NP_982272.2:p.His793Tyr
|
|
