ENST00000393943.10:c.*413G>A
MANE Select
|
ENSP00000377517.4:n.*413G>A
|
|
ENST00000635916.2:n.4627G>A
|
|
|
ENST00000636340.1:c.*1633G>A
|
ENSP00000490002.1:n.*1633G>A
|
|
ENST00000636408.1:n.1588G>A
|
|
|
ENST00000636573.1:c.*413G>A
|
ENSP00000490320.1:n.*413G>A
|
|
ENST00000637044.1:c.*1558G>A
|
ENSP00000490684.1:n.*1558G>A
|
|
ENST00000638112.1:c.*413G>A
|
ENSP00000489839.1:n.*413G>A
|
|
ENST00000638159.1:c.*413G>A
|
ENSP00000490360.1:n.*413G>A
|
|
ENST00000393943.9:c.*413G>A
|
ENSP00000377517.4:n.*413G>A
|
|
ENST00000428797.7:c.*413G>A
|
ENSP00000393097.2:n.*413G>A
|
|
ENST00000437025.6:c.*413G>A
|
ENSP00000415441.2:n.*413G>A
|
|
NM_000806.5:c.*413G>A
|
NP_000797.2:n.*413G>A
|
|
NM_001127643.1:c.*413G>A
|
NP_001121115.1:n.*413G>A
|
|
NM_001127644.1:c.*413G>A
|
NP_001121116.1:n.*413G>A
|
|
NM_001127645.1:c.*413G>A
|
NP_001121117.1:n.*413G>A
|
|
NM_001127648.1:c.*413G>A
|
NP_001121120.1:n.*413G>A
|
|
NM_001127644.2:c.*413G>A
MANE Select
|
NP_001121116.1:n.*413G>A
|
|
NM_001127643.2:c.*413G>A
|
NP_001121115.1:n.*413G>A
|
|
NM_001127645.2:c.*413G>A
|
NP_001121117.1:n.*413G>A
|
|
NM_001127648.2:c.*413G>A
|
NP_001121120.1:n.*413G>A
|
|