ENST00000687337.1:c.*1131T>C
|
ENSP00000508998.1:n.*1131T>C
|
|
ENST00000688199.1:c.1397T>C
|
ENSP00000510237.1:p.Leu466Ser
|
|
ENST00000691179.1:c.1460T>C
|
ENSP00000509010.1:p.Leu487Ser
|
|
ENST00000691970.1:c.*912T>C
|
ENSP00000508440.1:n.*912T>C
|
|
ENST00000692497.1:c.1535T>C
|
ENSP00000509870.1:p.Leu512Ser
|
|
ENST00000692988.1:n.1353T>C
|
|
|
ENST00000269143.8:c.1535T>C
MANE Select
|
ENSP00000269143.2:p.Leu512Ser
|
|
ENST00000269143.7:c.1535T>C
|
ENSP00000269143.2:p.Leu512Ser
|
|
NM_006796.2:c.1535T>C , LRG_666t1:c.1535T>C
|
NP_006787.2:p.Leu512Ser
|
|
XM_011525601.1:c.1535T>C
|
XP_011523903.1:p.Leu512Ser
|
|
XM_011525601.3:c.1535T>C
|
XP_011523903.1:p.Leu512Ser
|
|
NM_006796.3:c.1535T>C
MANE Select
|
NP_006787.2:p.Leu512Ser
|
|