ENST00000356141.9:c.1789C>T
MANE Select
|
ENSP00000348460.4:p.His597Tyr
|
|
ENST00000551634.6:c.1798C>T
|
ENSP00000448373.2:p.His600Tyr
|
|
ENST00000680362.1:c.1689C>T
|
|
|
ENST00000681323.1:c.793+2515C>T
|
|
|
ENST00000346562.6:c.1693C>T
|
ENSP00000319610.5:p.His565Tyr
|
|
ENST00000356141.8:c.1789C>T
|
ENSP00000348460.4:p.His597Tyr
|
|
ENST00000357798.9:c.1750C>T
|
ENSP00000350446.5:p.His584Tyr
|
|
ENST00000548645.5:c.1699C>T
|
ENSP00000448916.1:p.His567Tyr
|
|
ENST00000551492.5:c.1804C>T
|
ENSP00000450392.1:p.His602Tyr
|
|
ENST00000551634.5:c.1711C>T
|
ENSP00000448373.1:p.His571Tyr
|
|
NM_001164749.1:c.1789C>T
|
NP_001158221.1:p.His597Tyr
|
|
NM_001165893.1:c.1699C>T
|
NP_001159365.1:p.His567Tyr
|
|
NM_022123.2:c.1693C>T
|
NP_071406.1:p.His565Tyr
|
|
NM_173159.2:c.1750C>T
|
NP_775182.1:p.His584Tyr
|
|
XM_005267991.2:c.1810C>T
|
XP_005268048.1:p.His604Tyr
|
|
XM_005267992.2:c.1804C>T
|
XP_005268049.1:p.His602Tyr
|
|
XM_005267993.2:c.1750C>T
|
XP_005268050.1:p.His584Tyr
|
|
XM_011537067.1:c.1840C>T
|
XP_011535369.1:p.His614Tyr
|
|
XM_011537068.1:c.1831C>T
|
XP_011535370.1:p.His611Tyr
|
|
XM_011537069.1:c.1801C>T
|
XP_011535371.1:p.His601Tyr
|
|
XM_011537070.1:c.1744C>T
|
XP_011535372.1:p.His582Tyr
|
|
XM_011537071.1:c.1711C>T
|
XP_011535373.1:p.His571Tyr
|
|
XM_011537072.1:c.1690C>T
|
XP_011535374.1:p.His564Tyr
|
|
XM_011537073.1:c.1483C>T
|
XP_011535375.1:p.His495Tyr
|
|
XM_011537074.1:c.1483C>T
|
XP_011535376.1:p.His495Tyr
|
|
XM_005267991.3:c.1897C>T
|
XP_005268048.2:p.His633Tyr
|
|
XM_005267992.3:c.1891C>T
|
XP_005268049.2:p.His631Tyr
|
|
XM_011537067.2:c.1840C>T
|
XP_011535369.1:p.His614Tyr
|
|
XM_011537069.2:c.1888C>T
|
XP_011535371.2:p.His630Tyr
|
|
XM_011537070.2:c.1744C>T
|
XP_011535372.1:p.His582Tyr
|
|
XM_011537071.2:c.1798C>T
|
XP_011535373.2:p.His600Tyr
|
|
XM_011537072.2:c.1690C>T
|
XP_011535374.1:p.His564Tyr
|
|
XM_017021582.1:c.1948C>T
|
XP_016877071.1:p.His650Tyr
|
|
XM_017021583.1:c.1939C>T
|
XP_016877072.1:p.His647Tyr
|
|
XM_017021584.1:c.1858C>T
|
XP_016877073.1:p.His620Tyr
|
|
XM_017021585.1:c.1807C>T
|
XP_016877074.1:p.His603Tyr
|
|
XM_017021586.1:c.1483C>T
|
XP_016877075.1:p.His495Tyr
|
|
XM_017021587.1:c.1483C>T
|
XP_016877076.1:p.His495Tyr
|
|
XM_017021588.1:c.1483C>T
|
XP_016877077.1:p.His495Tyr
|
|
NM_001164749.2:c.1789C>T
MANE Select
|
NP_001158221.1:p.His597Tyr
|
|
NM_001165893.2:c.1699C>T
|
NP_001159365.1:p.His567Tyr
|
|
NM_022123.3:c.1693C>T
|
NP_071406.1:p.His565Tyr
|
|
NM_173159.3:c.1750C>T
|
NP_775182.1:p.His584Tyr
|
|
NM_001394988.1:c.1744C>T
|
NP_001381917.1:p.His582Tyr
|
|
NM_001394989.1:c.1690C>T
|
NP_001381918.1:p.His564Tyr
|
|