ENST00000356141.9:c.2014G>T
MANE Select
|
ENSP00000348460.4:p.Glu672Ter
|
|
ENST00000551634.6:c.2023G>T
|
ENSP00000448373.2:p.Glu675Ter
|
|
ENST00000680362.1:c.1914G>T
|
|
|
ENST00000681323.1:c.793+2740G>T
|
|
|
ENST00000346562.6:c.1918G>T
|
ENSP00000319610.5:p.Glu640Ter
|
|
ENST00000356141.8:c.2014G>T
|
ENSP00000348460.4:p.Glu672Ter
|
|
ENST00000357798.9:c.1975G>T
|
ENSP00000350446.5:p.Glu659Ter
|
|
ENST00000548645.5:c.1924G>T
|
ENSP00000448916.1:p.Glu642Ter
|
|
ENST00000551492.5:c.2029G>T
|
ENSP00000450392.1:p.Glu677Ter
|
|
ENST00000551634.5:c.1936G>T
|
ENSP00000448373.1:p.Glu646Ter
|
|
NM_001164749.1:c.2014G>T
|
NP_001158221.1:p.Glu672Ter
|
|
NM_001165893.1:c.1924G>T
|
NP_001159365.1:p.Glu642Ter
|
|
NM_022123.2:c.1918G>T
|
NP_071406.1:p.Glu640Ter
|
|
NM_173159.2:c.1975G>T
|
NP_775182.1:p.Glu659Ter
|
|
XM_005267991.2:c.2035G>T
|
XP_005268048.1:p.Glu679Ter
|
|
XM_005267992.2:c.2029G>T
|
XP_005268049.1:p.Glu677Ter
|
|
XM_005267993.2:c.1975G>T
|
XP_005268050.1:p.Glu659Ter
|
|
XM_011537067.1:c.2065G>T
|
XP_011535369.1:p.Glu689Ter
|
|
XM_011537068.1:c.2056G>T
|
XP_011535370.1:p.Glu686Ter
|
|
XM_011537069.1:c.2026G>T
|
XP_011535371.1:p.Glu676Ter
|
|
XM_011537070.1:c.1969G>T
|
XP_011535372.1:p.Glu657Ter
|
|
XM_011537071.1:c.1936G>T
|
XP_011535373.1:p.Glu646Ter
|
|
XM_011537072.1:c.1915G>T
|
XP_011535374.1:p.Glu639Ter
|
|
XM_011537073.1:c.1708G>T
|
XP_011535375.1:p.Glu570Ter
|
|
XM_011537074.1:c.1708G>T
|
XP_011535376.1:p.Glu570Ter
|
|
XM_005267991.3:c.2122G>T
|
XP_005268048.2:p.Glu708Ter
|
|
XM_005267992.3:c.2116G>T
|
XP_005268049.2:p.Glu706Ter
|
|
XM_011537067.2:c.2065G>T
|
XP_011535369.1:p.Glu689Ter
|
|
XM_011537069.2:c.2113G>T
|
XP_011535371.2:p.Glu705Ter
|
|
XM_011537070.2:c.1969G>T
|
XP_011535372.1:p.Glu657Ter
|
|
XM_011537071.2:c.2023G>T
|
XP_011535373.2:p.Glu675Ter
|
|
XM_011537072.2:c.1915G>T
|
XP_011535374.1:p.Glu639Ter
|
|
XM_017021582.1:c.2173G>T
|
XP_016877071.1:p.Glu725Ter
|
|
XM_017021583.1:c.2164G>T
|
XP_016877072.1:p.Glu722Ter
|
|
XM_017021584.1:c.2083G>T
|
XP_016877073.1:p.Glu695Ter
|
|
XM_017021585.1:c.2032G>T
|
XP_016877074.1:p.Glu678Ter
|
|
XM_017021586.1:c.1708G>T
|
XP_016877075.1:p.Glu570Ter
|
|
XM_017021587.1:c.1708G>T
|
XP_016877076.1:p.Glu570Ter
|
|
XM_017021588.1:c.1708G>T
|
XP_016877077.1:p.Glu570Ter
|
|
NM_001164749.2:c.2014G>T
MANE Select
|
NP_001158221.1:p.Glu672Ter
|
|
NM_001165893.2:c.1924G>T
|
NP_001159365.1:p.Glu642Ter
|
|
NM_022123.3:c.1918G>T
|
NP_071406.1:p.Glu640Ter
|
|
NM_173159.3:c.1975G>T
|
NP_775182.1:p.Glu659Ter
|
|
NM_001394988.1:c.1969G>T
|
NP_001381917.1:p.Glu657Ter
|
|
NM_001394989.1:c.1915G>T
|
NP_001381918.1:p.Glu639Ter
|
|