ENST00000687337.1:c.*1124G>T
|
ENSP00000508998.1:n.*1124G>T
|
|
ENST00000688199.1:c.1390G>T
|
ENSP00000510237.1:p.Ala464Ser
|
|
ENST00000691179.1:c.1453G>T
|
ENSP00000509010.1:p.Ala485Ser
|
|
ENST00000691970.1:c.*905G>T
|
ENSP00000508440.1:n.*905G>T
|
|
ENST00000692497.1:c.1528G>T
|
ENSP00000509870.1:p.Ala510Ser
|
|
ENST00000692988.1:n.1346G>T
|
|
|
ENST00000269143.8:c.1528G>T
MANE Select
|
ENSP00000269143.2:p.Ala510Ser
|
|
ENST00000269143.7:c.1528G>T
|
ENSP00000269143.2:p.Ala510Ser
|
|
NM_006796.2:c.1528G>T , LRG_666t1:c.1528G>T
|
NP_006787.2:p.Ala510Ser
|
|
XM_011525601.1:c.1528G>T
|
XP_011523903.1:p.Ala510Ser
|
|
XM_011525601.3:c.1528G>T
|
XP_011523903.1:p.Ala510Ser
|
|
NM_006796.3:c.1528G>T
MANE Select
|
NP_006787.2:p.Ala510Ser
|
|