ENST00000261769.10:c.1947T>G
MANE Select
|
ENSP00000261769.4:p.Ser649=
|
|
ENST00000261769.9:c.1947T>G
|
ENSP00000261769.4:p.Ser649=
|
|
ENST00000422392.6:c.1764T>G
|
ENSP00000414946.2:p.Ser588=
|
|
ENST00000562118.1:n.165T>G
|
|
|
ENST00000562836.5:n.2018T>G
|
|
|
ENST00000566510.5:c.*613T>G
|
ENSP00000458139.1:n.*613T>G
|
|
ENST00000566612.5:c.*187T>G
|
ENSP00000454782.1:n.*187T>G
|
|
ENST00000611625.4:c.2010T>G
|
ENSP00000481063.1:p.Ser670=
|
|
ENST00000612417.4:c.1830+1290T>G
|
ENSP00000478360.1:n.1830+1290T>G
|
|
ENST00000621016.4:c.1865+1255T>G
|
ENSP00000480664.1:n.1865+1255T>G
|
|
NM_004360.3:c.1947T>G , LRG_301t1:c.1947T>G
|
NP_004351.1:p.Ser649=
|
|
XM_011523488.1:c.1212T>G
|
XP_011521790.1:p.Ser404=
|
|
XM_011523489.1:c.1212T>G
|
XP_011521791.1:p.Ser404=
|
|
NM_001317184.1:c.1764T>G
|
NP_001304113.1:p.Ser588=
|
|
NM_001317185.1:c.399T>G
|
NP_001304114.1:p.Ser133=
|
|
NM_001317186.1:c.-19T>G
|
NP_001304115.1:n.-19T>G
|
|
NM_004360.4:c.1947T>G
|
NP_004351.1:p.Ser649=
|
|
NM_004360.5:c.1947T>G
MANE Select
|
NP_004351.1:p.Ser649=
|
|
NM_001317184.2:c.1764T>G
|
NP_001304113.1:p.Ser588=
|
|
NM_001317185.2:c.399T>G
|
NP_001304114.1:p.Ser133=
|
|
NM_001317186.2:c.-19T>G
|
NP_001304115.1:n.-19T>G
|
|