ENST00000706989.1:c.2141C>T
|
ENSP00000516702.1:p.Thr714Met
|
|
ENST00000359125.7:c.2087C>T
MANE Select
|
ENSP00000352035.2:p.Thr696Met
|
|
ENST00000637193.1:c.1484C>T
|
ENSP00000490734.1:p.Thr495Met
|
|
ENST00000344462.8:c.1994C>T
|
ENSP00000339611.4:p.Thr665Met
|
|
ENST00000357249.6:c.1655C>T
|
ENSP00000349789.3:p.Thr552Met
|
|
ENST00000359125.6:c.2087C>T
|
ENSP00000352035.2:p.Thr696Met
|
|
ENST00000360480.7:c.2003C>T
|
ENSP00000353668.3:p.Thr668Met
|
|
ENST00000370224.5:c.2111C>T
|
ENSP00000359244.2:p.Thr704Met
|
|
ENST00000625514.2:c.2075C>T
|
ENSP00000486040.1:p.Thr692Met
|
|
ENST00000626839.2:c.2033C>T
|
ENSP00000486706.1:p.Thr678Met
|
|
ENST00000629241.2:c.2003C>T
|
ENSP00000487142.1:p.Thr668Met
|
|
ENST00000629676.2:c.1679+6274C>T
|
ENSP00000486194.1:n.1679+6274C>T
|
|
NM_004518.4:c.2003C>T
|
NP_004509.2:p.Thr668Met
|
|
NM_172106.1:c.2033C>T
|
NP_742104.1:p.Thr678Met
|
|
NM_172107.2:c.2087C>T
|
NP_742105.1:p.Thr696Met
|
|
NM_172108.3:c.1994C>T
|
NP_742106.1:p.Thr665Met
|
|
XM_006723787.1:c.2129C>T
|
XP_006723850.1:p.Thr710Met
|
|
XM_011528807.1:c.2195C>T
|
XP_011527109.1:p.Thr732Met
|
|
XM_011528808.1:c.2192C>T
|
XP_011527110.1:p.Thr731Met
|
|
XM_011528809.1:c.2165C>T
|
XP_011527111.1:p.Thr722Met
|
|
XM_011528810.1:c.2141C>T
|
XP_011527112.1:p.Thr714Met
|
|
XM_011528811.1:c.2111C>T
|
XP_011527113.1:p.Thr704Met
|
|
XM_011528812.1:c.2084C>T
|
XP_011527114.1:p.Thr695Met
|
|
XM_011528813.1:c.2069C>T
|
XP_011527115.1:p.Thr690Met
|
|
XM_011528814.1:c.1676C>T
|
XP_011527116.1:p.Thr559Met
|
|
NM_004518.5:c.2003C>T
|
NP_004509.2:p.Thr668Met
|
|
NM_172106.2:c.2033C>T
|
NP_742104.1:p.Thr678Met
|
|
NM_172107.3:c.2087C>T
|
NP_742105.1:p.Thr696Met
|
|
NM_172108.4:c.1994C>T
|
NP_742106.1:p.Thr665Met
|
|
XM_011528810.2:c.2141C>T
|
XP_011527112.1:p.Thr714Met
|
|
XM_011528811.2:c.2111C>T
|
XP_011527113.1:p.Thr704Met
|
|
XM_017027841.2:c.2138C>T
|
XP_016883330.1:p.Thr713Met
|
|
XM_017027842.2:c.2075C>T
|
XP_016883331.1:p.Thr692Met
|
|
XM_017027843.1:c.2072C>T
|
XP_016883332.1:p.Thr691Met
|
|
XM_017027844.2:c.2030C>T
|
XP_016883333.1:p.Thr677Met
|
|
XM_017027845.1:c.1103C>T
|
XP_016883334.1:p.Thr368Met
|
|
NM_004518.6:c.2003C>T
|
NP_004509.2:p.Thr668Met
|
|
NM_172106.3:c.2033C>T
|
NP_742104.1:p.Thr678Met
|
|
NM_172107.4:c.2087C>T
MANE Select
|
NP_742105.1:p.Thr696Met
|
|
NM_172108.5:c.1994C>T
|
NP_742106.1:p.Thr665Met
|
|
NM_001382235.1:c.2141C>T
|
NP_001369164.1:p.Thr714Met
|
|