|
NM_001127178.3:c.2872G>T
MANE Select
|
NP_001120650.1:p.Glu958Ter
|
|
ENST00000453061.7:c.2872G>T
MANE Select
|
ENSP00000415203.2:p.Glu958Ter
|
|
NM_001127178.2:c.2872G>T
|
NP_001120650.1:p.Glu958Ter
|
|
NM_001289051.1:c.2605G>T
|
NP_001275980.1:p.Glu869Ter
|
|
NM_001289051.2:c.2605G>T
|
NP_001275980.1:p.Glu869Ter
|
|
NM_001289052.1:c.2473G>T
|
NP_001275981.1:p.Glu825Ter
|
|
NM_001289052.2:c.2473G>T
|
NP_001275981.1:p.Glu825Ter
|
|
NM_001345986.1:c.2605G>T
|
NP_001332915.1:p.Glu869Ter
|
|
NM_001345986.2:c.2605G>T
|
NP_001332915.1:p.Glu869Ter
|
|
NM_001345987.1:c.2581G>T
|
NP_001332916.1:p.Glu861Ter
|
|
NM_001345987.2:c.2581G>T
|
NP_001332916.1:p.Glu861Ter
|
|
NM_001345988.1:c.1843G>T
|
NP_001332917.1:p.Glu615Ter
|
|
NM_001345988.2:c.1843G>T
|
NP_001332917.1:p.Glu615Ter
|
|
NM_001345990.1:c.1339G>T
|
NP_001332919.1:p.Glu447Ter
|
|
NM_001345990.2:c.1339G>T
|
NP_001332919.1:p.Glu447Ter
|
|
NM_001345991.1:c.1339G>T
|
NP_001332920.1:p.Glu447Ter
|
|
NM_001345991.2:c.1339G>T
|
NP_001332920.1:p.Glu447Ter
|
|
NM_001345994.1:c.1774G>T
|
NP_001332923.1:p.Glu592Ter
|
|
NM_001345994.2:c.1774G>T
|
NP_001332923.1:p.Glu592Ter
|
|
NM_017733.4:c.2848G>T
|
NP_060203.3:p.Glu950Ter
|
|
NM_017733.5:c.2848G>T
|
NP_060203.3:p.Glu950Ter
|
|
NR_110293.1:n.2962G>T
|
|
|
NR_110293.2:n.2952G>T
|
|
|
NR_144326.1:n.3877G>T
|
|
|
NR_144326.2:n.3867G>T
|
|
|
NR_144327.1:n.3265G>T
|
|
|
NR_144327.2:n.3255G>T
|
|
|
NR_144328.1:n.3431G>T
|
|
|
NR_144328.2:n.3421G>T
|
|
|
NR_144329.1:n.2936G>T
|
|
|
NR_144329.2:n.2926G>T
|
|
|
NR_144330.1:n.2698G>T
|
|
|
NR_144330.2:n.2688G>T
|
|
|
NR_144331.1:n.2934G>T
|
|
|
NR_144331.2:n.2924G>T
|
|
|
NR_144332.1:n.2553G>T
|
|
|
NR_144332.2:n.2543G>T
|
|
|
NR_144333.1:n.2243G>T
|
|
|
NR_144333.2:n.2233G>T
|
|
|
NR_144334.1:n.2433G>T
|
|
|
NR_144334.2:n.2423G>T
|
|
|
ENST00000310340.9:c.2848G>T
|
ENSP00000311750.5:p.Glu950Ter
|
|
ENST00000383028.8:c.2473G>T
|
ENSP00000372494.4:p.Glu825Ter
|
|
ENST00000453061.6:c.2872G>T
|
ENSP00000415203.2:p.Glu958Ter
|
|
ENST00000504346.5:c.2605G>T
|
ENSP00000424800.1:p.Glu869Ter
|
|
ENST00000505800.1:n.210G>T
|
|
|
ENST00000508144.1:n.487G>T
|
|
|
ENST00000511666.5:n.582G>T
|
|
|
ENST00000513192.1:n.2005G>T
|
|
|
ENST00000513239.5:n.3279G>T
|
|
|
ENST00000515237.1:n.421G>T
|
|
|
XM_005272283.2:c.2662G>T
|
XP_005272340.1:p.Glu888Ter
|
|
XM_005272284.2:c.2605G>T
|
XP_005272341.1:p.Glu869Ter
|
|
XM_011513491.1:c.2506G>T
|
XP_011511793.1:p.Glu836Ter
|
|
XM_011513491.2:c.2506G>T
|
XP_011511793.1:p.Glu836Ter
|
|
XM_011513492.1:c.1798G>T
|
XP_011511794.1:p.Glu600Ter
|
|
XR_001741251.2:n.3651G>T
|
|
|
XR_001741253.2:n.3389G>T
|
|
|
XR_001741254.2:n.8999G>T
|
|
|
XR_001741255.2:n.2722G>T
|
|
|
XR_001741258.2:n.2558G>T
|
|
|
XR_001741261.2:n.8760G>T
|
|
|
XR_001741262.2:n.2836G>T
|
|
|
XR_002959736.1:n.4598G>T
|
|
|
XR_002959737.1:n.10807G>T
|
|
|
XR_002959738.1:n.10732G>T
|
|
|
XR_924963.1:n.3641G>T
|
|
|
XR_924965.1:n.5996G>T
|
|
|
XR_924965.3:n.5972G>T
|
|
|
XR_924966.1:n.2698G>T
|
|
|
XR_924967.3:n.6313G>T
|
|
|
XR_924972.3:n.2412G>T
|
|
