ENST00000261769.10:c.2081T>A
MANE Select
|
ENSP00000261769.4:p.Val694Asp
|
|
ENST00000261769.9:c.2081T>A
|
ENSP00000261769.4:p.Val694Asp
|
|
ENST00000422392.6:c.1898T>A
|
ENSP00000414946.2:p.Val633Asp
|
|
ENST00000562118.1:n.299T>A
|
|
|
ENST00000562836.5:n.2152T>A
|
|
|
ENST00000566510.5:c.*747T>A
|
ENSP00000458139.1:n.*747T>A
|
|
ENST00000566612.5:c.*321T>A
|
ENSP00000454782.1:n.*321T>A
|
|
ENST00000611625.4:c.2144T>A
|
ENSP00000481063.1:p.Val715Asp
|
|
ENST00000612417.4:c.1830+1424T>A
|
ENSP00000478360.1:n.1830+1424T>A
|
|
ENST00000621016.4:c.1865+1389T>A
|
ENSP00000480664.1:n.1865+1389T>A
|
|
NM_004360.3:c.2081T>A , LRG_301t1:c.2081T>A
|
NP_004351.1:p.Val694Asp
|
|
XM_011523488.1:c.1346T>A
|
XP_011521790.1:p.Val449Asp
|
|
XM_011523489.1:c.1346T>A
|
XP_011521791.1:p.Val449Asp
|
|
NM_001317184.1:c.1898T>A
|
NP_001304113.1:p.Val633Asp
|
|
NM_001317185.1:c.533T>A
|
NP_001304114.1:p.Val178Asp
|
|
NM_001317186.1:c.116T>A
|
NP_001304115.1:p.Val39Asp
|
|
NM_004360.4:c.2081T>A
|
NP_004351.1:p.Val694Asp
|
|
NM_004360.5:c.2081T>A
MANE Select
|
NP_004351.1:p.Val694Asp
|
|
NM_001317184.2:c.1898T>A
|
NP_001304113.1:p.Val633Asp
|
|
NM_001317185.2:c.533T>A
|
NP_001304114.1:p.Val178Asp
|
|
NM_001317186.2:c.116T>A
|
NP_001304115.1:p.Val39Asp
|
|