ENST00000706989.1:c.2434G>T
|
ENSP00000516702.1:p.Asp812Tyr
|
|
ENST00000359125.7:c.2380G>T
MANE Select
|
ENSP00000352035.2:p.Asp794Tyr
|
|
ENST00000637193.1:c.1777G>T
|
ENSP00000490734.1:p.Asp593Tyr
|
|
ENST00000344462.8:c.2287G>T
|
ENSP00000339611.4:p.Asp763Tyr
|
|
ENST00000357249.6:c.1948G>T
|
ENSP00000349789.3:p.Asp650Tyr
|
|
ENST00000359125.6:c.2380G>T
|
ENSP00000352035.2:p.Asp794Tyr
|
|
ENST00000360480.7:c.2296G>T
|
ENSP00000353668.3:p.Asp766Tyr
|
|
ENST00000370224.5:c.2241+163G>T
|
ENSP00000359244.2:n.2241+163G>T
|
|
ENST00000625514.2:c.2205+163G>T
|
ENSP00000486040.1:n.2205+163G>T
|
|
ENST00000626839.2:c.2326G>T
|
ENSP00000486706.1:p.Asp776Tyr
|
|
ENST00000629241.2:c.2133+163G>T
|
ENSP00000487142.1:n.2133+163G>T
|
|
ENST00000629676.2:c.1680-6040G>T
|
ENSP00000486194.1:n.1680-6040G>T
|
|
NM_004518.4:c.2296G>T
|
NP_004509.2:p.Asp766Tyr
|
|
NM_172106.1:c.2326G>T
|
NP_742104.1:p.Asp776Tyr
|
|
NM_172107.2:c.2380G>T
|
NP_742105.1:p.Asp794Tyr
|
|
NM_172108.3:c.2287G>T
|
NP_742106.1:p.Asp763Tyr
|
|
XM_006723787.1:c.2422G>T
|
XP_006723850.1:p.Asp808Tyr
|
|
XM_011528807.1:c.2488G>T
|
XP_011527109.1:p.Asp830Tyr
|
|
XM_011528808.1:c.2485G>T
|
XP_011527110.1:p.Asp829Tyr
|
|
XM_011528809.1:c.2458G>T
|
XP_011527111.1:p.Asp820Tyr
|
|
XM_011528810.1:c.2434G>T
|
XP_011527112.1:p.Asp812Tyr
|
|
XM_011528811.1:c.2404G>T
|
XP_011527113.1:p.Asp802Tyr
|
|
XM_011528812.1:c.2377G>T
|
XP_011527114.1:p.Asp793Tyr
|
|
XM_011528813.1:c.2362G>T
|
XP_011527115.1:p.Asp788Tyr
|
|
XM_011528814.1:c.1969G>T
|
XP_011527116.1:p.Asp657Tyr
|
|
NM_004518.5:c.2296G>T
|
NP_004509.2:p.Asp766Tyr
|
|
NM_172106.2:c.2326G>T
|
NP_742104.1:p.Asp776Tyr
|
|
NM_172107.3:c.2380G>T
|
NP_742105.1:p.Asp794Tyr
|
|
NM_172108.4:c.2287G>T
|
NP_742106.1:p.Asp763Tyr
|
|
XM_011528810.2:c.2434G>T
|
XP_011527112.1:p.Asp812Tyr
|
|
XM_011528811.2:c.2404G>T
|
XP_011527113.1:p.Asp802Tyr
|
|
XM_017027841.2:c.2431G>T
|
XP_016883330.1:p.Asp811Tyr
|
|
XM_017027842.2:c.2368G>T
|
XP_016883331.1:p.Asp790Tyr
|
|
XM_017027843.1:c.2365G>T
|
XP_016883332.1:p.Asp789Tyr
|
|
XM_017027844.2:c.2323G>T
|
XP_016883333.1:p.Asp775Tyr
|
|
XM_017027845.1:c.1396G>T
|
XP_016883334.1:p.Asp466Tyr
|
|
NM_004518.6:c.2296G>T
|
NP_004509.2:p.Asp766Tyr
|
|
NM_172106.3:c.2326G>T
|
NP_742104.1:p.Asp776Tyr
|
|
NM_172107.4:c.2380G>T
MANE Select
|
NP_742105.1:p.Asp794Tyr
|
|
NM_172108.5:c.2287G>T
|
NP_742106.1:p.Asp763Tyr
|
|
NM_001382235.1:c.2434G>T
|
NP_001369164.1:p.Asp812Tyr
|
|