ENST00000706989.1:c.2644G>T
|
ENSP00000516702.1:p.Asp882Tyr
|
|
ENST00000359125.7:c.2590G>T
MANE Select
|
ENSP00000352035.2:p.Asp864Tyr
|
|
ENST00000637193.1:c.1987G>T
|
ENSP00000490734.1:p.Asp663Tyr
|
|
ENST00000344462.8:c.2497G>T
|
ENSP00000339611.4:p.Asp833Tyr
|
|
ENST00000357249.6:c.2158G>T
|
ENSP00000349789.3:p.Asp720Tyr
|
|
ENST00000359125.6:c.2590G>T
|
ENSP00000352035.2:p.Asp864Tyr
|
|
ENST00000360480.7:c.2506G>T
|
ENSP00000353668.3:p.Asp836Tyr
|
|
ENST00000370224.5:c.2241+373G>T
|
ENSP00000359244.2:n.2241+373G>T
|
|
ENST00000625514.2:c.2205+373G>T
|
ENSP00000486040.1:n.2205+373G>T
|
|
ENST00000626839.2:c.2536G>T
|
ENSP00000486706.1:p.Asp846Tyr
|
|
ENST00000629241.2:c.2133+373G>T
|
ENSP00000487142.1:n.2133+373G>T
|
|
ENST00000629676.2:c.1680-5830G>T
|
ENSP00000486194.1:n.1680-5830G>T
|
|
NM_004518.4:c.2506G>T
|
NP_004509.2:p.Asp836Tyr
|
|
NM_172106.1:c.2536G>T
|
NP_742104.1:p.Asp846Tyr
|
|
NM_172107.2:c.2590G>T
|
NP_742105.1:p.Asp864Tyr
|
|
NM_172108.3:c.2497G>T
|
NP_742106.1:p.Asp833Tyr
|
|
XM_006723787.1:c.2632G>T
|
XP_006723850.1:p.Asp878Tyr
|
|
XM_011528807.1:c.2698G>T
|
XP_011527109.1:p.Asp900Tyr
|
|
XM_011528808.1:c.2695G>T
|
XP_011527110.1:p.Asp899Tyr
|
|
XM_011528809.1:c.2668G>T
|
XP_011527111.1:p.Asp890Tyr
|
|
XM_011528810.1:c.2644G>T
|
XP_011527112.1:p.Asp882Tyr
|
|
XM_011528811.1:c.2614G>T
|
XP_011527113.1:p.Asp872Tyr
|
|
XM_011528812.1:c.2587G>T
|
XP_011527114.1:p.Asp863Tyr
|
|
XM_011528813.1:c.2572G>T
|
XP_011527115.1:p.Asp858Tyr
|
|
XM_011528814.1:c.2179G>T
|
XP_011527116.1:p.Asp727Tyr
|
|
NM_004518.5:c.2506G>T
|
NP_004509.2:p.Asp836Tyr
|
|
NM_172106.2:c.2536G>T
|
NP_742104.1:p.Asp846Tyr
|
|
NM_172107.3:c.2590G>T
|
NP_742105.1:p.Asp864Tyr
|
|
NM_172108.4:c.2497G>T
|
NP_742106.1:p.Asp833Tyr
|
|
XM_011528810.2:c.2644G>T
|
XP_011527112.1:p.Asp882Tyr
|
|
XM_011528811.2:c.2614G>T
|
XP_011527113.1:p.Asp872Tyr
|
|
XM_017027841.2:c.2641G>T
|
XP_016883330.1:p.Asp881Tyr
|
|
XM_017027842.2:c.2578G>T
|
XP_016883331.1:p.Asp860Tyr
|
|
XM_017027843.1:c.2575G>T
|
XP_016883332.1:p.Asp859Tyr
|
|
XM_017027844.2:c.2533G>T
|
XP_016883333.1:p.Asp845Tyr
|
|
XM_017027845.1:c.1606G>T
|
XP_016883334.1:p.Asp536Tyr
|
|
NM_004518.6:c.2506G>T
|
NP_004509.2:p.Asp836Tyr
|
|
NM_172106.3:c.2536G>T
|
NP_742104.1:p.Asp846Tyr
|
|
NM_172107.4:c.2590G>T
MANE Select
|
NP_742105.1:p.Asp864Tyr
|
|
NM_172108.5:c.2497G>T
|
NP_742106.1:p.Asp833Tyr
|
|
NM_001382235.1:c.2644G>T
|
NP_001369164.1:p.Asp882Tyr
|
|