ENST00000477226.6:n.520T>A
|
|
|
ENST00000683013.1:n.434T>A
|
|
|
ENST00000373960.4:c.1046T>A
MANE Select
|
ENSP00000363071.3:p.Met349Lys
|
|
ENST00000373960.3:c.1046T>A
|
ENSP00000363071.3:p.Met349Lys
|
|
ENST00000477226.5:n.518T>A
|
|
|
ENST00000492726.1:n.441T>A
|
|
|
NM_001927.3:c.1046T>A , LRG_380t1:c.1046T>A
|
NP_001918.3:p.Met349Lys
|
|
NM_001927.4:c.1046T>A
MANE Select
|
NP_001918.3:p.Met349Lys
|
|
NM_001382708.1:c.1043T>A
|
NP_001369637.1:p.Met348Lys
|
|
NM_001382709.1:c.736-122T>A
|
NP_001369638.1:n.736-122T>A
|
|
NM_001382710.1:c.1024-47T>A
|
NP_001369639.1:n.1024-47T>A
|
|
NM_001382711.1:c.1025T>A
|
NP_001369640.1:p.Met342Lys
|
|
NM_001382712.1:c.1046T>A
|
NP_001369641.1:p.Met349Lys
|
|
NM_001382713.1:c.776T>A
|
NP_001369642.1:p.Met259Lys
|
|