ENST00000706989.1:c.2341A>G
|
ENSP00000516702.1:p.Met781Val
|
|
ENST00000359125.7:c.2287A>G
MANE Select
|
ENSP00000352035.2:p.Met763Val
|
|
ENST00000637193.1:c.1684A>G
|
ENSP00000490734.1:p.Met562Val
|
|
ENST00000344462.8:c.2194A>G
|
ENSP00000339611.4:p.Met732Val
|
|
ENST00000357249.6:c.1855A>G
|
ENSP00000349789.3:p.Met619Val
|
|
ENST00000359125.6:c.2287A>G
|
ENSP00000352035.2:p.Met763Val
|
|
ENST00000360480.7:c.2203A>G
|
ENSP00000353668.3:p.Met735Val
|
|
ENST00000370224.5:c.2241+70A>G
|
ENSP00000359244.2:n.2241+70A>G
|
|
ENST00000625514.2:c.2205+70A>G
|
ENSP00000486040.1:n.2205+70A>G
|
|
ENST00000626839.2:c.2233A>G
|
ENSP00000486706.1:p.Met745Val
|
|
ENST00000629241.2:c.2133+70A>G
|
ENSP00000487142.1:n.2133+70A>G
|
|
ENST00000629676.2:c.1680-6133A>G
|
ENSP00000486194.1:n.1680-6133A>G
|
|
NM_004518.4:c.2203A>G
|
NP_004509.2:p.Met735Val
|
|
NM_172106.1:c.2233A>G
|
NP_742104.1:p.Met745Val
|
|
NM_172107.2:c.2287A>G
|
NP_742105.1:p.Met763Val
|
|
NM_172108.3:c.2194A>G
|
NP_742106.1:p.Met732Val
|
|
XM_006723787.1:c.2329A>G
|
XP_006723850.1:p.Met777Val
|
|
XM_011528807.1:c.2395A>G
|
XP_011527109.1:p.Met799Val
|
|
XM_011528808.1:c.2392A>G
|
XP_011527110.1:p.Met798Val
|
|
XM_011528809.1:c.2365A>G
|
XP_011527111.1:p.Met789Val
|
|
XM_011528810.1:c.2341A>G
|
XP_011527112.1:p.Met781Val
|
|
XM_011528811.1:c.2311A>G
|
XP_011527113.1:p.Met771Val
|
|
XM_011528812.1:c.2284A>G
|
XP_011527114.1:p.Met762Val
|
|
XM_011528813.1:c.2269A>G
|
XP_011527115.1:p.Met757Val
|
|
XM_011528814.1:c.1876A>G
|
XP_011527116.1:p.Met626Val
|
|
NM_004518.5:c.2203A>G
|
NP_004509.2:p.Met735Val
|
|
NM_172106.2:c.2233A>G
|
NP_742104.1:p.Met745Val
|
|
NM_172107.3:c.2287A>G
|
NP_742105.1:p.Met763Val
|
|
NM_172108.4:c.2194A>G
|
NP_742106.1:p.Met732Val
|
|
XM_011528810.2:c.2341A>G
|
XP_011527112.1:p.Met781Val
|
|
XM_011528811.2:c.2311A>G
|
XP_011527113.1:p.Met771Val
|
|
XM_017027841.2:c.2338A>G
|
XP_016883330.1:p.Met780Val
|
|
XM_017027842.2:c.2275A>G
|
XP_016883331.1:p.Met759Val
|
|
XM_017027843.1:c.2272A>G
|
XP_016883332.1:p.Met758Val
|
|
XM_017027844.2:c.2230A>G
|
XP_016883333.1:p.Met744Val
|
|
XM_017027845.1:c.1303A>G
|
XP_016883334.1:p.Met435Val
|
|
NM_004518.6:c.2203A>G
|
NP_004509.2:p.Met735Val
|
|
NM_172106.3:c.2233A>G
|
NP_742104.1:p.Met745Val
|
|
NM_172107.4:c.2287A>G
MANE Select
|
NP_742105.1:p.Met763Val
|
|
NM_172108.5:c.2194A>G
|
NP_742106.1:p.Met732Val
|
|
NM_001382235.1:c.2341A>G
|
NP_001369164.1:p.Met781Val
|
|