ENST00000356141.9:c.2180G>A
MANE Select
|
ENSP00000348460.4:p.Arg727His
|
|
ENST00000551634.6:c.2189G>A
|
ENSP00000448373.2:p.Arg730His
|
|
ENST00000680362.1:c.2080G>A
|
|
|
ENST00000681323.1:c.793+2906G>A
|
|
|
ENST00000346562.6:c.2084G>A
|
ENSP00000319610.5:p.Arg695His
|
|
ENST00000356141.8:c.2180G>A
|
ENSP00000348460.4:p.Arg727His
|
|
ENST00000357798.9:c.2141G>A
|
ENSP00000350446.5:p.Arg714His
|
|
ENST00000548645.5:c.2090G>A
|
ENSP00000448916.1:p.Arg697His
|
|
ENST00000551492.5:c.2195G>A
|
ENSP00000450392.1:p.Arg732His
|
|
ENST00000551634.5:c.2102G>A
|
ENSP00000448373.1:p.Arg701His
|
|
NM_001164749.1:c.2180G>A
|
NP_001158221.1:p.Arg727His
|
|
NM_001165893.1:c.2090G>A
|
NP_001159365.1:p.Arg697His
|
|
NM_022123.2:c.2084G>A
|
NP_071406.1:p.Arg695His
|
|
NM_173159.2:c.2141G>A
|
NP_775182.1:p.Arg714His
|
|
XM_005267991.2:c.2201G>A
|
XP_005268048.1:p.Arg734His
|
|
XM_005267992.2:c.2195G>A
|
XP_005268049.1:p.Arg732His
|
|
XM_005267993.2:c.2141G>A
|
XP_005268050.1:p.Arg714His
|
|
XM_011537067.1:c.2231G>A
|
XP_011535369.1:p.Arg744His
|
|
XM_011537068.1:c.2222G>A
|
XP_011535370.1:p.Arg741His
|
|
XM_011537069.1:c.2192G>A
|
XP_011535371.1:p.Arg731His
|
|
XM_011537070.1:c.2135G>A
|
XP_011535372.1:p.Arg712His
|
|
XM_011537071.1:c.2102G>A
|
XP_011535373.1:p.Arg701His
|
|
XM_011537072.1:c.2081G>A
|
XP_011535374.1:p.Arg694His
|
|
XM_011537073.1:c.1874G>A
|
XP_011535375.1:p.Arg625His
|
|
XM_011537074.1:c.1874G>A
|
XP_011535376.1:p.Arg625His
|
|
XM_005267991.3:c.2288G>A
|
XP_005268048.2:p.Arg763His
|
|
XM_005267992.3:c.2282G>A
|
XP_005268049.2:p.Arg761His
|
|
XM_011537067.2:c.2231G>A
|
XP_011535369.1:p.Arg744His
|
|
XM_011537069.2:c.2279G>A
|
XP_011535371.2:p.Arg760His
|
|
XM_011537070.2:c.2135G>A
|
XP_011535372.1:p.Arg712His
|
|
XM_011537071.2:c.2189G>A
|
XP_011535373.2:p.Arg730His
|
|
XM_011537072.2:c.2081G>A
|
XP_011535374.1:p.Arg694His
|
|
XM_017021582.1:c.2339G>A
|
XP_016877071.1:p.Arg780His
|
|
XM_017021583.1:c.2330G>A
|
XP_016877072.1:p.Arg777His
|
|
XM_017021584.1:c.2249G>A
|
XP_016877073.1:p.Arg750His
|
|
XM_017021585.1:c.2198G>A
|
XP_016877074.1:p.Arg733His
|
|
XM_017021586.1:c.1874G>A
|
XP_016877075.1:p.Arg625His
|
|
XM_017021587.1:c.1874G>A
|
XP_016877076.1:p.Arg625His
|
|
XM_017021588.1:c.1874G>A
|
XP_016877077.1:p.Arg625His
|
|
NM_001164749.2:c.2180G>A
MANE Select
|
NP_001158221.1:p.Arg727His
|
|
NM_001165893.2:c.2090G>A
|
NP_001159365.1:p.Arg697His
|
|
NM_022123.3:c.2084G>A
|
NP_071406.1:p.Arg695His
|
|
NM_173159.3:c.2141G>A
|
NP_775182.1:p.Arg714His
|
|
NM_001394988.1:c.2135G>A
|
NP_001381917.1:p.Arg712His
|
|
NM_001394989.1:c.2081G>A
|
NP_001381918.1:p.Arg694His
|
|