ENST00000706989.1:c.2453G>T
|
ENSP00000516702.1:p.Arg818Leu
|
|
ENST00000359125.7:c.2399G>T
MANE Select
|
ENSP00000352035.2:p.Arg800Leu
|
|
ENST00000637193.1:c.1796G>T
|
ENSP00000490734.1:p.Arg599Leu
|
|
ENST00000344462.8:c.2306G>T
|
ENSP00000339611.4:p.Arg769Leu
|
|
ENST00000357249.6:c.1967G>T
|
ENSP00000349789.3:p.Arg656Leu
|
|
ENST00000359125.6:c.2399G>T
|
ENSP00000352035.2:p.Arg800Leu
|
|
ENST00000360480.7:c.2315G>T
|
ENSP00000353668.3:p.Arg772Leu
|
|
ENST00000370224.5:c.2241+182G>T
|
ENSP00000359244.2:n.2241+182G>T
|
|
ENST00000625514.2:c.2205+182G>T
|
ENSP00000486040.1:n.2205+182G>T
|
|
ENST00000626839.2:c.2345G>T
|
ENSP00000486706.1:p.Arg782Leu
|
|
ENST00000629241.2:c.2133+182G>T
|
ENSP00000487142.1:n.2133+182G>T
|
|
ENST00000629676.2:c.1680-6021G>T
|
ENSP00000486194.1:n.1680-6021G>T
|
|
NM_004518.4:c.2315G>T
|
NP_004509.2:p.Arg772Leu
|
|
NM_172106.1:c.2345G>T
|
NP_742104.1:p.Arg782Leu
|
|
NM_172107.2:c.2399G>T
|
NP_742105.1:p.Arg800Leu
|
|
NM_172108.3:c.2306G>T
|
NP_742106.1:p.Arg769Leu
|
|
XM_006723787.1:c.2441G>T
|
XP_006723850.1:p.Arg814Leu
|
|
XM_011528807.1:c.2507G>T
|
XP_011527109.1:p.Arg836Leu
|
|
XM_011528808.1:c.2504G>T
|
XP_011527110.1:p.Arg835Leu
|
|
XM_011528809.1:c.2477G>T
|
XP_011527111.1:p.Arg826Leu
|
|
XM_011528810.1:c.2453G>T
|
XP_011527112.1:p.Arg818Leu
|
|
XM_011528811.1:c.2423G>T
|
XP_011527113.1:p.Arg808Leu
|
|
XM_011528812.1:c.2396G>T
|
XP_011527114.1:p.Arg799Leu
|
|
XM_011528813.1:c.2381G>T
|
XP_011527115.1:p.Arg794Leu
|
|
XM_011528814.1:c.1988G>T
|
XP_011527116.1:p.Arg663Leu
|
|
NM_004518.5:c.2315G>T
|
NP_004509.2:p.Arg772Leu
|
|
NM_172106.2:c.2345G>T
|
NP_742104.1:p.Arg782Leu
|
|
NM_172107.3:c.2399G>T
|
NP_742105.1:p.Arg800Leu
|
|
NM_172108.4:c.2306G>T
|
NP_742106.1:p.Arg769Leu
|
|
XM_011528810.2:c.2453G>T
|
XP_011527112.1:p.Arg818Leu
|
|
XM_011528811.2:c.2423G>T
|
XP_011527113.1:p.Arg808Leu
|
|
XM_017027841.2:c.2450G>T
|
XP_016883330.1:p.Arg817Leu
|
|
XM_017027842.2:c.2387G>T
|
XP_016883331.1:p.Arg796Leu
|
|
XM_017027843.1:c.2384G>T
|
XP_016883332.1:p.Arg795Leu
|
|
XM_017027844.2:c.2342G>T
|
XP_016883333.1:p.Arg781Leu
|
|
XM_017027845.1:c.1415G>T
|
XP_016883334.1:p.Arg472Leu
|
|
NM_004518.6:c.2315G>T
|
NP_004509.2:p.Arg772Leu
|
|
NM_172106.3:c.2345G>T
|
NP_742104.1:p.Arg782Leu
|
|
NM_172107.4:c.2399G>T
MANE Select
|
NP_742105.1:p.Arg800Leu
|
|
NM_172108.5:c.2306G>T
|
NP_742106.1:p.Arg769Leu
|
|
NM_001382235.1:c.2453G>T
|
NP_001369164.1:p.Arg818Leu
|
|