ENST00000706989.1:c.1989G=
|
ENSP00000516702.1:p.Met663=
|
|
ENST00000359125.7:c.1935G=
MANE Select
|
ENSP00000352035.2:p.Met645=
|
|
ENST00000637193.1:c.1332G=
|
ENSP00000490734.1:p.Met444=
|
|
ENST00000637338.1:n.92G=
|
|
|
ENST00000344462.8:c.1842G=
|
ENSP00000339611.4:p.Met614=
|
|
ENST00000357249.6:c.1503G=
|
ENSP00000349789.3:p.Met501=
|
|
ENST00000359125.6:c.1935G=
|
ENSP00000352035.2:p.Met645=
|
|
ENST00000360480.7:c.1851G=
|
ENSP00000353668.3:p.Met617=
|
|
ENST00000370224.5:c.1959G=
|
ENSP00000359244.2:p.Met653=
|
|
ENST00000625514.2:c.1923G=
|
ENSP00000486040.1:p.Met641=
|
|
ENST00000626839.2:c.1881G=
|
ENSP00000486706.1:p.Met627=
|
|
ENST00000629241.2:c.1851G=
|
ENSP00000487142.1:p.Met617=
|
|
ENST00000629676.2:c.1679+6122G=
|
ENSP00000486194.1:n.1679+6122G=
|
|
NM_004518.4:c.1851G=
|
NP_004509.2:p.Met617=
|
|
NM_172106.1:c.1881G=
|
NP_742104.1:p.Met627=
|
|
NM_172107.2:c.1935G=
|
NP_742105.1:p.Met645=
|
|
NM_172108.3:c.1842G=
|
NP_742106.1:p.Met614=
|
|
XM_006723787.1:c.1977G=
|
XP_006723850.1:p.Met659=
|
|
XM_011528807.1:c.2043G=
|
XP_011527109.1:p.Met681=
|
|
XM_011528808.1:c.2040G=
|
XP_011527110.1:p.Met680=
|
|
XM_011528809.1:c.2013G=
|
XP_011527111.1:p.Met671=
|
|
XM_011528810.1:c.1989G=
|
XP_011527112.1:p.Met663=
|
|
XM_011528811.1:c.1959G=
|
XP_011527113.1:p.Met653=
|
|
XM_011528812.1:c.1932G=
|
XP_011527114.1:p.Met644=
|
|
XM_011528813.1:c.1917G=
|
XP_011527115.1:p.Met639=
|
|
XM_011528814.1:c.1524G=
|
XP_011527116.1:p.Met508=
|
|
NM_004518.5:c.1851G=
|
NP_004509.2:p.Met617=
|
|
NM_172106.2:c.1881G=
|
NP_742104.1:p.Met627=
|
|
NM_172107.3:c.1935G=
|
NP_742105.1:p.Met645=
|
|
NM_172108.4:c.1842G=
|
NP_742106.1:p.Met614=
|
|
XM_011528810.2:c.1989G=
|
XP_011527112.1:p.Met663=
|
|
XM_011528811.2:c.1959G=
|
XP_011527113.1:p.Met653=
|
|
XM_017027841.2:c.1986G=
|
XP_016883330.1:p.Met662=
|
|
XM_017027842.2:c.1923G=
|
XP_016883331.1:p.Met641=
|
|
XM_017027843.1:c.1920G=
|
XP_016883332.1:p.Met640=
|
|
XM_017027844.2:c.1878G=
|
XP_016883333.1:p.Met626=
|
|
XM_017027845.1:c.951G=
|
XP_016883334.1:p.Met317=
|
|
NM_004518.6:c.1851G=
|
NP_004509.2:p.Met617=
|
|
NM_172106.3:c.1881G=
|
NP_742104.1:p.Met627=
|
|
NM_172107.4:c.1935G=
MANE Select
|
NP_742105.1:p.Met645=
|
|
NM_172108.5:c.1842G=
|
NP_742106.1:p.Met614=
|
|
NM_001382235.1:c.1989G=
|
NP_001369164.1:p.Met663=
|
|