ENST00000477226.6:n.815G>T
|
|
|
ENST00000683013.1:n.729G>T
|
|
|
ENST00000373960.4:c.1341G>T
MANE Select
|
ENSP00000363071.3:p.Met447Ile
|
|
ENST00000373960.3:c.1341G>T
|
ENSP00000363071.3:p.Met447Ile
|
|
ENST00000483395.1:n.196G>T
|
|
|
NM_001927.3:c.1341G>T , LRG_380t1:c.1341G>T
|
NP_001918.3:p.Met447Ile
|
|
NM_001927.4:c.1341G>T
MANE Select
|
NP_001918.3:p.Met447Ile
|
|
NM_001382708.1:c.1338G>T
|
NP_001369637.1:p.Met446Ile
|
|
NM_001382709.1:c.909G>T
|
NP_001369638.1:p.Met303Ile
|
|
NM_001382710.1:c.1272G>T
|
NP_001369639.1:p.Met424Ile
|
|
NM_001382711.1:c.1320G>T
|
NP_001369640.1:p.Met440Ile
|
|
NM_001382712.1:c.1341G>T
|
NP_001369641.1:p.Met447Ile
|
|
NM_001382713.1:c.1071G>T
|
NP_001369642.1:p.Met357Ile
|
|