|
ENST00000261769.10:c.2487T>A
MANE Select
|
ENSP00000261769.4:p.Ser829=
|
|
|
ENST00000261769.9:c.2487T>A
|
ENSP00000261769.4:p.Ser829=
|
|
|
ENST00000422392.6:c.2304T>A
|
ENSP00000414946.2:p.Ser768=
|
|
|
ENST00000562118.1:n.705T>A
|
|
|
|
ENST00000562836.5:n.2558T>A
|
|
|
|
ENST00000566510.5:c.*1153T>A
|
ENSP00000458139.1:n.*1153T>A
|
|
|
ENST00000566612.5:c.*727T>A
|
ENSP00000454782.1:n.*727T>A
|
|
|
ENST00000611625.4:c.2550T>A
|
ENSP00000481063.1:p.Ser850=
|
|
|
ENST00000612417.4:c.1854-854T>A
|
ENSP00000478360.1:n.1854-854T>A
|
|
|
ENST00000621016.4:c.1866-866T>A
|
ENSP00000480664.1:n.1866-866T>A
|
|
|
NM_004360.3:c.2487T>A , LRG_301t1:c.2487T>A
|
NP_004351.1:p.Ser829=
|
|
|
XM_011523488.1:c.1752T>A
|
XP_011521790.1:p.Ser584=
|
|
|
XM_011523489.1:c.1752T>A
|
XP_011521791.1:p.Ser584=
|
|
|
NM_001317184.1:c.2304T>A
|
NP_001304113.1:p.Ser768=
|
|
|
NM_001317185.1:c.939T>A
|
NP_001304114.1:p.Ser313=
|
|
|
NM_001317186.1:c.522T>A
|
NP_001304115.1:p.Ser174=
|
|
|
NM_004360.4:c.2487T>A
|
NP_004351.1:p.Ser829=
|
|
|
NM_004360.5:c.2487T>A
MANE Select
|
NP_004351.1:p.Ser829=
|
|
|
NM_001317184.2:c.2304T>A
|
NP_001304113.1:p.Ser768=
|
|
|
NM_001317185.2:c.939T>A
|
NP_001304114.1:p.Ser313=
|
|
|
NM_001317186.2:c.522T>A
|
NP_001304115.1:p.Ser174=
|
|
