ENST00000338639.10:c.*213G>T
MANE Select
|
ENSP00000340278.5:n.*213G>T
|
|
ENST00000338639.9:c.*213G>T
|
ENSP00000340278.5:n.*213G>T
|
|
ENST00000377493.9:c.*213G>T
|
ENSP00000466242.1:n.*213G>T
|
|
ENST00000469225.1:c.696G>T
|
ENSP00000466756.1:n.696G>T
|
|
ENST00000493678.5:c.*213G>T
|
ENSP00000418770.1:n.*213G>T
|
|
NM_001123377.1:c.*213G>T
|
NP_001116849.1:n.*213G>T
|
|
NM_007262.4:c.*213G>T
|
NP_009193.2:n.*213G>T
|
|
XM_005263424.2:c.*213G>T
|
XP_005263481.1:n.*213G>T
|
|
XM_005263424.3:c.*213G>T
|
XP_005263481.1:n.*213G>T
|
|
NM_007262.5:c.*213G>T
MANE Select
|
NP_009193.2:n.*213G>T
|
|
NM_001123377.2:c.*213G>T
|
NP_001116849.1:n.*213G>T
|
|