ENST00000706989.1:c.2453G=
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ENSP00000516702.1:p.Arg818=
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|
ENST00000359125.7:c.2399G=
MANE Select
|
ENSP00000352035.2:p.Arg800=
|
|
ENST00000637193.1:c.1796G=
|
ENSP00000490734.1:p.Arg599=
|
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ENST00000344462.8:c.2306G=
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ENSP00000339611.4:p.Arg769=
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ENST00000357249.6:c.1967G=
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ENSP00000349789.3:p.Arg656=
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ENST00000359125.6:c.2399G=
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ENSP00000352035.2:p.Arg800=
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ENST00000360480.7:c.2315G=
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ENSP00000353668.3:p.Arg772=
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ENST00000370224.5:c.2241+182G=
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ENSP00000359244.2:n.2241+182G=
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ENST00000625514.2:c.2205+182G=
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ENSP00000486040.1:n.2205+182G=
|
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ENST00000626839.2:c.2345G=
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ENSP00000486706.1:p.Arg782=
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ENST00000629241.2:c.2133+182G=
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ENSP00000487142.1:n.2133+182G=
|
|
ENST00000629676.2:c.1680-6021G=
|
ENSP00000486194.1:n.1680-6021G=
|
|
NM_004518.4:c.2315G=
|
NP_004509.2:p.Arg772=
|
|
NM_172106.1:c.2345G=
|
NP_742104.1:p.Arg782=
|
|
NM_172107.2:c.2399G=
|
NP_742105.1:p.Arg800=
|
|
NM_172108.3:c.2306G=
|
NP_742106.1:p.Arg769=
|
|
XM_006723787.1:c.2441G=
|
XP_006723850.1:p.Arg814=
|
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XM_011528807.1:c.2507G=
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XP_011527109.1:p.Arg836=
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XM_011528808.1:c.2504G=
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XP_011527110.1:p.Arg835=
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XM_011528809.1:c.2477G=
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XP_011527111.1:p.Arg826=
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XM_011528810.1:c.2453G=
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XP_011527112.1:p.Arg818=
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XM_011528811.1:c.2423G=
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XP_011527113.1:p.Arg808=
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XM_011528812.1:c.2396G=
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XP_011527114.1:p.Arg799=
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|
XM_011528813.1:c.2381G=
|
XP_011527115.1:p.Arg794=
|
|
XM_011528814.1:c.1988G=
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XP_011527116.1:p.Arg663=
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NM_004518.5:c.2315G=
|
NP_004509.2:p.Arg772=
|
|
NM_172106.2:c.2345G=
|
NP_742104.1:p.Arg782=
|
|
NM_172107.3:c.2399G=
|
NP_742105.1:p.Arg800=
|
|
NM_172108.4:c.2306G=
|
NP_742106.1:p.Arg769=
|
|
XM_011528810.2:c.2453G=
|
XP_011527112.1:p.Arg818=
|
|
XM_011528811.2:c.2423G=
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XP_011527113.1:p.Arg808=
|
|
XM_017027841.2:c.2450G=
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XP_016883330.1:p.Arg817=
|
|
XM_017027842.2:c.2387G=
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XP_016883331.1:p.Arg796=
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XM_017027843.1:c.2384G=
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XP_016883332.1:p.Arg795=
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XM_017027844.2:c.2342G=
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XP_016883333.1:p.Arg781=
|
|
XM_017027845.1:c.1415G=
|
XP_016883334.1:p.Arg472=
|
|
NM_004518.6:c.2315G=
|
NP_004509.2:p.Arg772=
|
|
NM_172106.3:c.2345G=
|
NP_742104.1:p.Arg782=
|
|
NM_172107.4:c.2399G=
MANE Select
|
NP_742105.1:p.Arg800=
|
|
NM_172108.5:c.2306G=
|
NP_742106.1:p.Arg769=
|
|
NM_001382235.1:c.2453G=
|
NP_001369164.1:p.Arg818=
|
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