ENST00000356141.9:c.1981G>T
MANE Select
|
ENSP00000348460.4:p.Asp661Tyr
|
|
ENST00000551634.6:c.1990G>T
|
ENSP00000448373.2:p.Asp664Tyr
|
|
ENST00000680362.1:c.1881G>T
|
|
|
ENST00000681323.1:c.793+2707G>T
|
|
|
ENST00000346562.6:c.1885G>T
|
ENSP00000319610.5:p.Asp629Tyr
|
|
ENST00000356141.8:c.1981G>T
|
ENSP00000348460.4:p.Asp661Tyr
|
|
ENST00000357798.9:c.1942G>T
|
ENSP00000350446.5:p.Asp648Tyr
|
|
ENST00000548645.5:c.1891G>T
|
ENSP00000448916.1:p.Asp631Tyr
|
|
ENST00000551492.5:c.1996G>T
|
ENSP00000450392.1:p.Asp666Tyr
|
|
ENST00000551634.5:c.1903G>T
|
ENSP00000448373.1:p.Asp635Tyr
|
|
NM_001164749.1:c.1981G>T
|
NP_001158221.1:p.Asp661Tyr
|
|
NM_001165893.1:c.1891G>T
|
NP_001159365.1:p.Asp631Tyr
|
|
NM_022123.2:c.1885G>T
|
NP_071406.1:p.Asp629Tyr
|
|
NM_173159.2:c.1942G>T
|
NP_775182.1:p.Asp648Tyr
|
|
XM_005267991.2:c.2002G>T
|
XP_005268048.1:p.Asp668Tyr
|
|
XM_005267992.2:c.1996G>T
|
XP_005268049.1:p.Asp666Tyr
|
|
XM_005267993.2:c.1942G>T
|
XP_005268050.1:p.Asp648Tyr
|
|
XM_011537067.1:c.2032G>T
|
XP_011535369.1:p.Asp678Tyr
|
|
XM_011537068.1:c.2023G>T
|
XP_011535370.1:p.Asp675Tyr
|
|
XM_011537069.1:c.1993G>T
|
XP_011535371.1:p.Asp665Tyr
|
|
XM_011537070.1:c.1936G>T
|
XP_011535372.1:p.Asp646Tyr
|
|
XM_011537071.1:c.1903G>T
|
XP_011535373.1:p.Asp635Tyr
|
|
XM_011537072.1:c.1882G>T
|
XP_011535374.1:p.Asp628Tyr
|
|
XM_011537073.1:c.1675G>T
|
XP_011535375.1:p.Asp559Tyr
|
|
XM_011537074.1:c.1675G>T
|
XP_011535376.1:p.Asp559Tyr
|
|
XM_005267991.3:c.2089G>T
|
XP_005268048.2:p.Asp697Tyr
|
|
XM_005267992.3:c.2083G>T
|
XP_005268049.2:p.Asp695Tyr
|
|
XM_011537067.2:c.2032G>T
|
XP_011535369.1:p.Asp678Tyr
|
|
XM_011537069.2:c.2080G>T
|
XP_011535371.2:p.Asp694Tyr
|
|
XM_011537070.2:c.1936G>T
|
XP_011535372.1:p.Asp646Tyr
|
|
XM_011537071.2:c.1990G>T
|
XP_011535373.2:p.Asp664Tyr
|
|
XM_011537072.2:c.1882G>T
|
XP_011535374.1:p.Asp628Tyr
|
|
XM_017021582.1:c.2140G>T
|
XP_016877071.1:p.Asp714Tyr
|
|
XM_017021583.1:c.2131G>T
|
XP_016877072.1:p.Asp711Tyr
|
|
XM_017021584.1:c.2050G>T
|
XP_016877073.1:p.Asp684Tyr
|
|
XM_017021585.1:c.1999G>T
|
XP_016877074.1:p.Asp667Tyr
|
|
XM_017021586.1:c.1675G>T
|
XP_016877075.1:p.Asp559Tyr
|
|
XM_017021587.1:c.1675G>T
|
XP_016877076.1:p.Asp559Tyr
|
|
XM_017021588.1:c.1675G>T
|
XP_016877077.1:p.Asp559Tyr
|
|
NM_001164749.2:c.1981G>T
MANE Select
|
NP_001158221.1:p.Asp661Tyr
|
|
NM_001165893.2:c.1891G>T
|
NP_001159365.1:p.Asp631Tyr
|
|
NM_022123.3:c.1885G>T
|
NP_071406.1:p.Asp629Tyr
|
|
NM_173159.3:c.1942G>T
|
NP_775182.1:p.Asp648Tyr
|
|
NM_001394988.1:c.1936G>T
|
NP_001381917.1:p.Asp646Tyr
|
|
NM_001394989.1:c.1882G>T
|
NP_001381918.1:p.Asp628Tyr
|
|