ENST00000477226.6:n.854T>C
|
|
|
ENST00000683013.1:n.768T>C
|
|
|
ENST00000373960.4:c.1380T>C
MANE Select
|
ENSP00000363071.3:p.Ser460=
|
|
ENST00000373960.3:c.1380T>C
|
ENSP00000363071.3:p.Ser460=
|
|
ENST00000483395.1:n.235T>C
|
|
|
NM_001927.3:c.1380T>C , LRG_380t1:c.1380T>C
|
NP_001918.3:p.Ser460=
|
|
NM_001927.4:c.1380T>C
MANE Select
|
NP_001918.3:p.Ser460=
|
|
NM_001382708.1:c.1377T>C
|
NP_001369637.1:p.Ser459=
|
|
NM_001382709.1:c.948T>C
|
NP_001369638.1:p.Ser316=
|
|
NM_001382710.1:c.1311T>C
|
NP_001369639.1:p.Ser437=
|
|
NM_001382711.1:c.1359T>C
|
NP_001369640.1:p.Ser453=
|
|
NM_001382712.1:c.1371+212T>C
|
NP_001369641.1:n.1371+212T>C
|
|
NM_001382713.1:c.1110T>C
|
NP_001369642.1:p.Ser370=
|
|