ENST00000329138.9:c.1785T>C
MANE Select
|
ENSP00000331201.4:p.Pro595=
|
|
ENST00000676462.1:c.1785T>C
|
ENSP00000503043.1:p.Pro595=
|
|
ENST00000676478.1:c.*1294T>C
|
ENSP00000504482.1:n.*1294T>C
|
|
ENST00000676546.1:c.1785T>C
|
ENSP00000504106.1:p.Pro595=
|
|
ENST00000676704.1:c.394T>C
|
|
|
ENST00000676729.1:c.1758T>C
|
ENSP00000503138.1:p.Pro586=
|
|
ENST00000677044.1:c.1785T>C
|
ENSP00000504151.1:p.Pro595=
|
|
ENST00000677109.1:c.1749T>C
|
ENSP00000503405.1:p.Pro583=
|
|
ENST00000677159.1:n.991T>C
|
|
|
ENST00000677161.1:c.1524T>C
|
ENSP00000503695.1:p.Pro508=
|
|
ENST00000677188.1:c.388T>C
|
|
|
ENST00000677225.1:c.1737T>C
|
ENSP00000503479.1:p.Pro579=
|
|
ENST00000677232.1:n.78T>C
|
|
|
ENST00000677243.1:c.1785T>C
|
ENSP00000502851.1:p.Pro595=
|
|
ENST00000677484.1:c.1803T>C
|
ENSP00000503188.1:p.Pro601=
|
|
ENST00000677728.1:c.171T>C
|
ENSP00000503213.1:p.Pro57=
|
|
ENST00000678096.1:c.1725T>C
|
ENSP00000504478.1:p.Pro575=
|
|
ENST00000678105.1:c.1584T>C
|
ENSP00000504789.1:p.Pro528=
|
|
ENST00000678115.1:n.2246T>C
|
|
|
ENST00000678176.1:c.213T>C
|
ENSP00000504798.1:p.Pro71=
|
|
ENST00000678196.1:c.1785T>C
|
ENSP00000503545.1:p.Pro595=
|
|
ENST00000678387.1:n.1996T>C
|
|
|
ENST00000678541.1:n.1629T>C
|
|
|
ENST00000678658.1:n.2242T>C
|
|
|
ENST00000678866.1:c.1839T>C
|
ENSP00000504854.1:p.Pro613=
|
|
ENST00000678896.1:c.78T>C
|
ENSP00000503714.1:p.Pro26=
|
|
ENST00000679036.1:c.78T>C
|
ENSP00000504505.1:p.Pro26=
|
|
ENST00000679191.1:c.1737T>C
|
ENSP00000503211.1:p.Pro579=
|
|
ENST00000679275.1:c.*848T>C
|
ENSP00000504270.1:n.*848T>C
|
|
ENST00000679336.1:c.1785T>C
|
ENSP00000502961.1:p.Pro595=
|
|
ENST00000329138.8:c.1785T>C
|
ENSP00000331201.4:p.Pro595=
|
|
ENST00000570355.1:n.301T>C
|
|
|
ENST00000571237.1:c.792T>C
|
ENSP00000458775.1:p.Pro264=
|
|
ENST00000571647.1:n.946T>C
|
|
|
ENST00000573949.1:n.344+372T>C
|
|
|
NM_004712.4:c.1785T>C
|
NP_004703.1:p.Pro595=
|
|
XM_005257794.2:c.1758T>C
|
XP_005257851.1:p.Pro586=
|
|
XM_011525463.1:c.1785T>C
|
XP_011523765.1:p.Pro595=
|
|
XM_011525464.1:c.1260T>C
|
XP_011523766.1:p.Pro420=
|
|
XM_011525463.2:c.1785T>C
|
XP_011523765.1:p.Pro595=
|
|
XM_017025297.1:c.1758T>C
|
XP_016880786.1:p.Pro586=
|
|
XM_017025298.1:c.1260T>C
|
XP_016880787.1:p.Pro420=
|
|
XM_024451024.1:c.1584T>C
|
XP_024306792.1:p.Pro528=
|
|
XM_024451025.1:c.1584T>C
|
XP_024306793.1:p.Pro528=
|
|
NM_004712.5:c.1785T>C
MANE Select
|
NP_004703.1:p.Pro595=
|
|