ENST00000706989.1:c.2304G>T
|
ENSP00000516702.1:p.Arg768=
|
|
ENST00000359125.7:c.2250G>T
MANE Select
|
ENSP00000352035.2:p.Arg750=
|
|
ENST00000637193.1:c.1647G>T
|
ENSP00000490734.1:p.Arg549=
|
|
ENST00000344462.8:c.2157G>T
|
ENSP00000339611.4:p.Arg719=
|
|
ENST00000357249.6:c.1818G>T
|
ENSP00000349789.3:p.Arg606=
|
|
ENST00000359125.6:c.2250G>T
|
ENSP00000352035.2:p.Arg750=
|
|
ENST00000360480.7:c.2166G>T
|
ENSP00000353668.3:p.Arg722=
|
|
ENST00000370224.5:c.2241+33G>T
|
ENSP00000359244.2:n.2241+33G>T
|
|
ENST00000625514.2:c.2205+33G>T
|
ENSP00000486040.1:n.2205+33G>T
|
|
ENST00000626839.2:c.2196G>T
|
ENSP00000486706.1:p.Arg732=
|
|
ENST00000629241.2:c.2133+33G>T
|
ENSP00000487142.1:n.2133+33G>T
|
|
ENST00000629676.2:c.1680-6170G>T
|
ENSP00000486194.1:n.1680-6170G>T
|
|
NM_004518.4:c.2166G>T
|
NP_004509.2:p.Arg722=
|
|
NM_172106.1:c.2196G>T
|
NP_742104.1:p.Arg732=
|
|
NM_172107.2:c.2250G>T
|
NP_742105.1:p.Arg750=
|
|
NM_172108.3:c.2157G>T
|
NP_742106.1:p.Arg719=
|
|
XM_006723787.1:c.2292G>T
|
XP_006723850.1:p.Arg764=
|
|
XM_011528807.1:c.2358G>T
|
XP_011527109.1:p.Arg786=
|
|
XM_011528808.1:c.2355G>T
|
XP_011527110.1:p.Arg785=
|
|
XM_011528809.1:c.2328G>T
|
XP_011527111.1:p.Arg776=
|
|
XM_011528810.1:c.2304G>T
|
XP_011527112.1:p.Arg768=
|
|
XM_011528811.1:c.2274G>T
|
XP_011527113.1:p.Arg758=
|
|
XM_011528812.1:c.2247G>T
|
XP_011527114.1:p.Arg749=
|
|
XM_011528813.1:c.2232G>T
|
XP_011527115.1:p.Arg744=
|
|
XM_011528814.1:c.1839G>T
|
XP_011527116.1:p.Arg613=
|
|
NM_004518.5:c.2166G>T
|
NP_004509.2:p.Arg722=
|
|
NM_172106.2:c.2196G>T
|
NP_742104.1:p.Arg732=
|
|
NM_172107.3:c.2250G>T
|
NP_742105.1:p.Arg750=
|
|
NM_172108.4:c.2157G>T
|
NP_742106.1:p.Arg719=
|
|
XM_011528810.2:c.2304G>T
|
XP_011527112.1:p.Arg768=
|
|
XM_011528811.2:c.2274G>T
|
XP_011527113.1:p.Arg758=
|
|
XM_017027841.2:c.2301G>T
|
XP_016883330.1:p.Arg767=
|
|
XM_017027842.2:c.2238G>T
|
XP_016883331.1:p.Arg746=
|
|
XM_017027843.1:c.2235G>T
|
XP_016883332.1:p.Arg745=
|
|
XM_017027844.2:c.2193G>T
|
XP_016883333.1:p.Arg731=
|
|
XM_017027845.1:c.1266G>T
|
XP_016883334.1:p.Arg422=
|
|
NM_004518.6:c.2166G>T
|
NP_004509.2:p.Arg722=
|
|
NM_172106.3:c.2196G>T
|
NP_742104.1:p.Arg732=
|
|
NM_172107.4:c.2250G>T
MANE Select
|
NP_742105.1:p.Arg750=
|
|
NM_172108.5:c.2157G>T
|
NP_742106.1:p.Arg719=
|
|
NM_001382235.1:c.2304G>T
|
NP_001369164.1:p.Arg768=
|
|