ENST00000706989.1:c.2527G>A
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ENSP00000516702.1:p.Ala843Thr
|
|
ENST00000359125.7:c.2473G>A
MANE Select
|
ENSP00000352035.2:p.Ala825Thr
|
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ENST00000637193.1:c.1870G>A
|
ENSP00000490734.1:p.Ala624Thr
|
|
ENST00000344462.8:c.2380G>A
|
ENSP00000339611.4:p.Ala794Thr
|
|
ENST00000357249.6:c.2041G>A
|
ENSP00000349789.3:p.Ala681Thr
|
|
ENST00000359125.6:c.2473G>A
|
ENSP00000352035.2:p.Ala825Thr
|
|
ENST00000360480.7:c.2389G>A
|
ENSP00000353668.3:p.Ala797Thr
|
|
ENST00000370224.5:c.2241+256G>A
|
ENSP00000359244.2:n.2241+256G>A
|
|
ENST00000625514.2:c.2205+256G>A
|
ENSP00000486040.1:n.2205+256G>A
|
|
ENST00000626839.2:c.2419G>A
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ENSP00000486706.1:p.Ala807Thr
|
|
ENST00000629241.2:c.2133+256G>A
|
ENSP00000487142.1:n.2133+256G>A
|
|
ENST00000629676.2:c.1680-5947G>A
|
ENSP00000486194.1:n.1680-5947G>A
|
|
NM_004518.4:c.2389G>A
|
NP_004509.2:p.Ala797Thr
|
|
NM_172106.1:c.2419G>A
|
NP_742104.1:p.Ala807Thr
|
|
NM_172107.2:c.2473G>A
|
NP_742105.1:p.Ala825Thr
|
|
NM_172108.3:c.2380G>A
|
NP_742106.1:p.Ala794Thr
|
|
XM_006723787.1:c.2515G>A
|
XP_006723850.1:p.Ala839Thr
|
|
XM_011528807.1:c.2581G>A
|
XP_011527109.1:p.Ala861Thr
|
|
XM_011528808.1:c.2578G>A
|
XP_011527110.1:p.Ala860Thr
|
|
XM_011528809.1:c.2551G>A
|
XP_011527111.1:p.Ala851Thr
|
|
XM_011528810.1:c.2527G>A
|
XP_011527112.1:p.Ala843Thr
|
|
XM_011528811.1:c.2497G>A
|
XP_011527113.1:p.Ala833Thr
|
|
XM_011528812.1:c.2470G>A
|
XP_011527114.1:p.Ala824Thr
|
|
XM_011528813.1:c.2455G>A
|
XP_011527115.1:p.Ala819Thr
|
|
XM_011528814.1:c.2062G>A
|
XP_011527116.1:p.Ala688Thr
|
|
NM_004518.5:c.2389G>A
|
NP_004509.2:p.Ala797Thr
|
|
NM_172106.2:c.2419G>A
|
NP_742104.1:p.Ala807Thr
|
|
NM_172107.3:c.2473G>A
|
NP_742105.1:p.Ala825Thr
|
|
NM_172108.4:c.2380G>A
|
NP_742106.1:p.Ala794Thr
|
|
XM_011528810.2:c.2527G>A
|
XP_011527112.1:p.Ala843Thr
|
|
XM_011528811.2:c.2497G>A
|
XP_011527113.1:p.Ala833Thr
|
|
XM_017027841.2:c.2524G>A
|
XP_016883330.1:p.Ala842Thr
|
|
XM_017027842.2:c.2461G>A
|
XP_016883331.1:p.Ala821Thr
|
|
XM_017027843.1:c.2458G>A
|
XP_016883332.1:p.Ala820Thr
|
|
XM_017027844.2:c.2416G>A
|
XP_016883333.1:p.Ala806Thr
|
|
XM_017027845.1:c.1489G>A
|
XP_016883334.1:p.Ala497Thr
|
|
NM_004518.6:c.2389G>A
|
NP_004509.2:p.Ala797Thr
|
|
NM_172106.3:c.2419G>A
|
NP_742104.1:p.Ala807Thr
|
|
NM_172107.4:c.2473G>A
MANE Select
|
NP_742105.1:p.Ala825Thr
|
|
NM_172108.5:c.2380G>A
|
NP_742106.1:p.Ala794Thr
|
|
NM_001382235.1:c.2527G>A
|
NP_001369164.1:p.Ala843Thr
|
|