ENST00000706989.1:c.1984T>C
|
ENSP00000516702.1:p.Tyr662His
|
|
ENST00000359125.7:c.1930T>C
MANE Select
|
ENSP00000352035.2:p.Tyr644His
|
|
ENST00000637193.1:c.1327T>C
|
ENSP00000490734.1:p.Tyr443His
|
|
ENST00000637338.1:n.87T>C
|
|
|
ENST00000344462.8:c.1837T>C
|
ENSP00000339611.4:p.Tyr613His
|
|
ENST00000357249.6:c.1498T>C
|
ENSP00000349789.3:p.Tyr500His
|
|
ENST00000359125.6:c.1930T>C
|
ENSP00000352035.2:p.Tyr644His
|
|
ENST00000360480.7:c.1846T>C
|
ENSP00000353668.3:p.Tyr616His
|
|
ENST00000370224.5:c.1954T>C
|
ENSP00000359244.2:p.Tyr652His
|
|
ENST00000625514.2:c.1918T>C
|
ENSP00000486040.1:p.Tyr640His
|
|
ENST00000626839.2:c.1876T>C
|
ENSP00000486706.1:p.Tyr626His
|
|
ENST00000629241.2:c.1846T>C
|
ENSP00000487142.1:p.Tyr616His
|
|
ENST00000629676.2:c.1679+6117T>C
|
ENSP00000486194.1:n.1679+6117T>C
|
|
NM_004518.4:c.1846T>C
|
NP_004509.2:p.Tyr616His
|
|
NM_172106.1:c.1876T>C
|
NP_742104.1:p.Tyr626His
|
|
NM_172107.2:c.1930T>C
|
NP_742105.1:p.Tyr644His
|
|
NM_172108.3:c.1837T>C
|
NP_742106.1:p.Tyr613His
|
|
XM_006723787.1:c.1972T>C
|
XP_006723850.1:p.Tyr658His
|
|
XM_011528807.1:c.2038T>C
|
XP_011527109.1:p.Tyr680His
|
|
XM_011528808.1:c.2035T>C
|
XP_011527110.1:p.Tyr679His
|
|
XM_011528809.1:c.2008T>C
|
XP_011527111.1:p.Tyr670His
|
|
XM_011528810.1:c.1984T>C
|
XP_011527112.1:p.Tyr662His
|
|
XM_011528811.1:c.1954T>C
|
XP_011527113.1:p.Tyr652His
|
|
XM_011528812.1:c.1927T>C
|
XP_011527114.1:p.Tyr643His
|
|
XM_011528813.1:c.1912T>C
|
XP_011527115.1:p.Tyr638His
|
|
XM_011528814.1:c.1519T>C
|
XP_011527116.1:p.Tyr507His
|
|
NM_004518.5:c.1846T>C
|
NP_004509.2:p.Tyr616His
|
|
NM_172106.2:c.1876T>C
|
NP_742104.1:p.Tyr626His
|
|
NM_172107.3:c.1930T>C
|
NP_742105.1:p.Tyr644His
|
|
NM_172108.4:c.1837T>C
|
NP_742106.1:p.Tyr613His
|
|
XM_011528810.2:c.1984T>C
|
XP_011527112.1:p.Tyr662His
|
|
XM_011528811.2:c.1954T>C
|
XP_011527113.1:p.Tyr652His
|
|
XM_017027841.2:c.1981T>C
|
XP_016883330.1:p.Tyr661His
|
|
XM_017027842.2:c.1918T>C
|
XP_016883331.1:p.Tyr640His
|
|
XM_017027843.1:c.1915T>C
|
XP_016883332.1:p.Tyr639His
|
|
XM_017027844.2:c.1873T>C
|
XP_016883333.1:p.Tyr625His
|
|
XM_017027845.1:c.946T>C
|
XP_016883334.1:p.Tyr316His
|
|
NM_004518.6:c.1846T>C
|
NP_004509.2:p.Tyr616His
|
|
NM_172106.3:c.1876T>C
|
NP_742104.1:p.Tyr626His
|
|
NM_172107.4:c.1930T>C
MANE Select
|
NP_742105.1:p.Tyr644His
|
|
NM_172108.5:c.1837T>C
|
NP_742106.1:p.Tyr613His
|
|
NM_001382235.1:c.1984T>C
|
NP_001369164.1:p.Tyr662His
|
|