ENST00000706989.1:c.2082C>G
|
ENSP00000516702.1:p.Ser694Arg
|
|
ENST00000359125.7:c.2028C>G
MANE Select
|
ENSP00000352035.2:p.Ser676Arg
|
|
ENST00000637193.1:c.1425C>G
|
ENSP00000490734.1:p.Ser475Arg
|
|
ENST00000344462.8:c.1935C>G
|
ENSP00000339611.4:p.Ser645Arg
|
|
ENST00000357249.6:c.1596C>G
|
ENSP00000349789.3:p.Ser532Arg
|
|
ENST00000359125.6:c.2028C>G
|
ENSP00000352035.2:p.Ser676Arg
|
|
ENST00000360480.7:c.1944C>G
|
ENSP00000353668.3:p.Ser648Arg
|
|
ENST00000370224.5:c.2052C>G
|
ENSP00000359244.2:p.Ser684Arg
|
|
ENST00000625514.2:c.2016C>G
|
ENSP00000486040.1:p.Ser672Arg
|
|
ENST00000626839.2:c.1974C>G
|
ENSP00000486706.1:p.Ser658Arg
|
|
ENST00000629241.2:c.1944C>G
|
ENSP00000487142.1:p.Ser648Arg
|
|
ENST00000629676.2:c.1679+6215C>G
|
ENSP00000486194.1:n.1679+6215C>G
|
|
NM_004518.4:c.1944C>G
|
NP_004509.2:p.Ser648Arg
|
|
NM_172106.1:c.1974C>G
|
NP_742104.1:p.Ser658Arg
|
|
NM_172107.2:c.2028C>G
|
NP_742105.1:p.Ser676Arg
|
|
NM_172108.3:c.1935C>G
|
NP_742106.1:p.Ser645Arg
|
|
XM_006723787.1:c.2070C>G
|
XP_006723850.1:p.Ser690Arg
|
|
XM_011528807.1:c.2136C>G
|
XP_011527109.1:p.Ser712Arg
|
|
XM_011528808.1:c.2133C>G
|
XP_011527110.1:p.Ser711Arg
|
|
XM_011528809.1:c.2106C>G
|
XP_011527111.1:p.Ser702Arg
|
|
XM_011528810.1:c.2082C>G
|
XP_011527112.1:p.Ser694Arg
|
|
XM_011528811.1:c.2052C>G
|
XP_011527113.1:p.Ser684Arg
|
|
XM_011528812.1:c.2025C>G
|
XP_011527114.1:p.Ser675Arg
|
|
XM_011528813.1:c.2010C>G
|
XP_011527115.1:p.Ser670Arg
|
|
XM_011528814.1:c.1617C>G
|
XP_011527116.1:p.Ser539Arg
|
|
NM_004518.5:c.1944C>G
|
NP_004509.2:p.Ser648Arg
|
|
NM_172106.2:c.1974C>G
|
NP_742104.1:p.Ser658Arg
|
|
NM_172107.3:c.2028C>G
|
NP_742105.1:p.Ser676Arg
|
|
NM_172108.4:c.1935C>G
|
NP_742106.1:p.Ser645Arg
|
|
XM_011528810.2:c.2082C>G
|
XP_011527112.1:p.Ser694Arg
|
|
XM_011528811.2:c.2052C>G
|
XP_011527113.1:p.Ser684Arg
|
|
XM_017027841.2:c.2079C>G
|
XP_016883330.1:p.Ser693Arg
|
|
XM_017027842.2:c.2016C>G
|
XP_016883331.1:p.Ser672Arg
|
|
XM_017027843.1:c.2013C>G
|
XP_016883332.1:p.Ser671Arg
|
|
XM_017027844.2:c.1971C>G
|
XP_016883333.1:p.Ser657Arg
|
|
XM_017027845.1:c.1044C>G
|
XP_016883334.1:p.Ser348Arg
|
|
NM_004518.6:c.1944C>G
|
NP_004509.2:p.Ser648Arg
|
|
NM_172106.3:c.1974C>G
|
NP_742104.1:p.Ser658Arg
|
|
NM_172107.4:c.2028C>G
MANE Select
|
NP_742105.1:p.Ser676Arg
|
|
NM_172108.5:c.1935C>G
|
NP_742106.1:p.Ser645Arg
|
|
NM_001382235.1:c.2082C>G
|
NP_001369164.1:p.Ser694Arg
|
|