ENST00000649046.1:c.2357T>A
MANE Select
|
ENSP00000496870.1:p.Val786Asp
|
|
ENST00000263816.7:c.2357T>A
|
ENSP00000263816.3:p.Val786Asp
|
|
ENST00000443831.1:c.1946T>A
|
ENSP00000409813.1:p.Val649Asp
|
|
NM_004525.2:c.2357T>A
|
NP_004516.2:p.Val786Asp
|
|
XM_011511183.1:c.2357T>A
|
XP_011509485.1:p.Val786Asp
|
|
XM_011511184.1:c.68T>A
|
XP_011509486.1:p.Val23Asp
|
|
XM_011511185.1:c.2357T>A
|
XP_011509487.1:p.Val786Asp
|
|
NM_004525.3:c.2357T>A
MANE Select
|
NP_004516.2:p.Val786Asp
|
|
XM_011511183.3:c.2357T>A
|
XP_011509485.1:p.Val786Asp
|
|
XM_011511184.2:c.68T>A
|
XP_011509486.1:p.Val23Asp
|
|