ENST00000706989.1:c.2035G>A
|
ENSP00000516702.1:p.Ala679Thr
|
|
ENST00000359125.7:c.1981G>A
MANE Select
|
ENSP00000352035.2:p.Ala661Thr
|
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ENST00000637193.1:c.1378G>A
|
ENSP00000490734.1:p.Ala460Thr
|
|
ENST00000344462.8:c.1888G>A
|
ENSP00000339611.4:p.Ala630Thr
|
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ENST00000357249.6:c.1549G>A
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ENSP00000349789.3:p.Ala517Thr
|
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ENST00000359125.6:c.1981G>A
|
ENSP00000352035.2:p.Ala661Thr
|
|
ENST00000360480.7:c.1897G>A
|
ENSP00000353668.3:p.Ala633Thr
|
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ENST00000370224.5:c.2005G>A
|
ENSP00000359244.2:p.Ala669Thr
|
|
ENST00000625514.2:c.1969G>A
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ENSP00000486040.1:p.Ala657Thr
|
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ENST00000626839.2:c.1927G>A
|
ENSP00000486706.1:p.Ala643Thr
|
|
ENST00000629241.2:c.1897G>A
|
ENSP00000487142.1:p.Ala633Thr
|
|
ENST00000629676.2:c.1679+6168G>A
|
ENSP00000486194.1:n.1679+6168G>A
|
|
NM_004518.4:c.1897G>A
|
NP_004509.2:p.Ala633Thr
|
|
NM_172106.1:c.1927G>A
|
NP_742104.1:p.Ala643Thr
|
|
NM_172107.2:c.1981G>A
|
NP_742105.1:p.Ala661Thr
|
|
NM_172108.3:c.1888G>A
|
NP_742106.1:p.Ala630Thr
|
|
XM_006723787.1:c.2023G>A
|
XP_006723850.1:p.Ala675Thr
|
|
XM_011528807.1:c.2089G>A
|
XP_011527109.1:p.Ala697Thr
|
|
XM_011528808.1:c.2086G>A
|
XP_011527110.1:p.Ala696Thr
|
|
XM_011528809.1:c.2059G>A
|
XP_011527111.1:p.Ala687Thr
|
|
XM_011528810.1:c.2035G>A
|
XP_011527112.1:p.Ala679Thr
|
|
XM_011528811.1:c.2005G>A
|
XP_011527113.1:p.Ala669Thr
|
|
XM_011528812.1:c.1978G>A
|
XP_011527114.1:p.Ala660Thr
|
|
XM_011528813.1:c.1963G>A
|
XP_011527115.1:p.Ala655Thr
|
|
XM_011528814.1:c.1570G>A
|
XP_011527116.1:p.Ala524Thr
|
|
NM_004518.5:c.1897G>A
|
NP_004509.2:p.Ala633Thr
|
|
NM_172106.2:c.1927G>A
|
NP_742104.1:p.Ala643Thr
|
|
NM_172107.3:c.1981G>A
|
NP_742105.1:p.Ala661Thr
|
|
NM_172108.4:c.1888G>A
|
NP_742106.1:p.Ala630Thr
|
|
XM_011528810.2:c.2035G>A
|
XP_011527112.1:p.Ala679Thr
|
|
XM_011528811.2:c.2005G>A
|
XP_011527113.1:p.Ala669Thr
|
|
XM_017027841.2:c.2032G>A
|
XP_016883330.1:p.Ala678Thr
|
|
XM_017027842.2:c.1969G>A
|
XP_016883331.1:p.Ala657Thr
|
|
XM_017027843.1:c.1966G>A
|
XP_016883332.1:p.Ala656Thr
|
|
XM_017027844.2:c.1924G>A
|
XP_016883333.1:p.Ala642Thr
|
|
XM_017027845.1:c.997G>A
|
XP_016883334.1:p.Ala333Thr
|
|
NM_004518.6:c.1897G>A
|
NP_004509.2:p.Ala633Thr
|
|
NM_172106.3:c.1927G>A
|
NP_742104.1:p.Ala643Thr
|
|
NM_172107.4:c.1981G>A
MANE Select
|
NP_742105.1:p.Ala661Thr
|
|
NM_172108.5:c.1888G>A
|
NP_742106.1:p.Ala630Thr
|
|
NM_001382235.1:c.2035G>A
|
NP_001369164.1:p.Ala679Thr
|
|