ENST00000706989.1:c.2388G>A
|
ENSP00000516702.1:p.Glu796=
|
|
ENST00000359125.7:c.2334G>A
MANE Select
|
ENSP00000352035.2:p.Glu778=
|
|
ENST00000637193.1:c.1731G>A
|
ENSP00000490734.1:p.Glu577=
|
|
ENST00000344462.8:c.2241G>A
|
ENSP00000339611.4:p.Glu747=
|
|
ENST00000357249.6:c.1902G>A
|
ENSP00000349789.3:p.Glu634=
|
|
ENST00000359125.6:c.2334G>A
|
ENSP00000352035.2:p.Glu778=
|
|
ENST00000360480.7:c.2250G>A
|
ENSP00000353668.3:p.Glu750=
|
|
ENST00000370224.5:c.2241+117G>A
|
ENSP00000359244.2:n.2241+117G>A
|
|
ENST00000625514.2:c.2205+117G>A
|
ENSP00000486040.1:n.2205+117G>A
|
|
ENST00000626839.2:c.2280G>A
|
ENSP00000486706.1:p.Glu760=
|
|
ENST00000629241.2:c.2133+117G>A
|
ENSP00000487142.1:n.2133+117G>A
|
|
ENST00000629676.2:c.1680-6086G>A
|
ENSP00000486194.1:n.1680-6086G>A
|
|
NM_004518.4:c.2250G>A
|
NP_004509.2:p.Glu750=
|
|
NM_172106.1:c.2280G>A
|
NP_742104.1:p.Glu760=
|
|
NM_172107.2:c.2334G>A
|
NP_742105.1:p.Glu778=
|
|
NM_172108.3:c.2241G>A
|
NP_742106.1:p.Glu747=
|
|
XM_006723787.1:c.2376G>A
|
XP_006723850.1:p.Glu792=
|
|
XM_011528807.1:c.2442G>A
|
XP_011527109.1:p.Glu814=
|
|
XM_011528808.1:c.2439G>A
|
XP_011527110.1:p.Glu813=
|
|
XM_011528809.1:c.2412G>A
|
XP_011527111.1:p.Glu804=
|
|
XM_011528810.1:c.2388G>A
|
XP_011527112.1:p.Glu796=
|
|
XM_011528811.1:c.2358G>A
|
XP_011527113.1:p.Glu786=
|
|
XM_011528812.1:c.2331G>A
|
XP_011527114.1:p.Glu777=
|
|
XM_011528813.1:c.2316G>A
|
XP_011527115.1:p.Glu772=
|
|
XM_011528814.1:c.1923G>A
|
XP_011527116.1:p.Glu641=
|
|
NM_004518.5:c.2250G>A
|
NP_004509.2:p.Glu750=
|
|
NM_172106.2:c.2280G>A
|
NP_742104.1:p.Glu760=
|
|
NM_172107.3:c.2334G>A
|
NP_742105.1:p.Glu778=
|
|
NM_172108.4:c.2241G>A
|
NP_742106.1:p.Glu747=
|
|
XM_011528810.2:c.2388G>A
|
XP_011527112.1:p.Glu796=
|
|
XM_011528811.2:c.2358G>A
|
XP_011527113.1:p.Glu786=
|
|
XM_017027841.2:c.2385G>A
|
XP_016883330.1:p.Glu795=
|
|
XM_017027842.2:c.2322G>A
|
XP_016883331.1:p.Glu774=
|
|
XM_017027843.1:c.2319G>A
|
XP_016883332.1:p.Glu773=
|
|
XM_017027844.2:c.2277G>A
|
XP_016883333.1:p.Glu759=
|
|
XM_017027845.1:c.1350G>A
|
XP_016883334.1:p.Glu450=
|
|
NM_004518.6:c.2250G>A
|
NP_004509.2:p.Glu750=
|
|
NM_172106.3:c.2280G>A
|
NP_742104.1:p.Glu760=
|
|
NM_172107.4:c.2334G>A
MANE Select
|
NP_742105.1:p.Glu778=
|
|
NM_172108.5:c.2241G>A
|
NP_742106.1:p.Glu747=
|
|
NM_001382235.1:c.2388G>A
|
NP_001369164.1:p.Glu796=
|
|