ENST00000261769.10:c.1936+499T>G
(CDH1)
MANE Select
|
ENSP00000261769.4:n.1936+499T>G
|
|
ENST00000261769.9:c.1936+499T>G
(CDH1)
|
ENSP00000261769.4:n.1936+499T>G
|
|
ENST00000422392.6:c.1753+499T>G
(CDH1)
|
ENSP00000414946.2:n.1753+499T>G
|
|
ENST00000562087.2:n.138T>G
(FTLP14)
|
|
|
ENST00000562836.5:n.2007+499T>G
(CDH1)
|
|
|
ENST00000566510.5:c.*602+499T>G
(CDH1)
|
ENSP00000458139.1:n.*602+499T>G
|
|
ENST00000566612.5:c.*176+499T>G
(CDH1)
|
ENSP00000454782.1:n.*176+499T>G
|
|
ENST00000611625.4:c.1999+499T>G
(CDH1)
|
ENSP00000481063.1:n.1999+499T>G
|
|
ENST00000612417.4:c.1830+605T>G
(CDH1)
|
ENSP00000478360.1:n.1830+605T>G
|
|
ENST00000621016.4:c.1865+570T>G
(CDH1)
|
ENSP00000480664.1:n.1865+570T>G
|
|
NM_004360.3:c.1936+499T>G , LRG_301t1:c.1936+499T>G
(CDH1)
|
NP_004351.1:n.1936+499T>G
|
|
XM_011523488.1:c.1201+499T>G
(CDH1)
|
XP_011521790.1:n.1201+499T>G
|
|
XM_011523489.1:c.1201+499T>G
(CDH1)
|
XP_011521791.1:n.1201+499T>G
|
|
NM_001317184.1:c.1753+499T>G
(CDH1)
|
NP_001304113.1:n.1753+499T>G
|
|
NM_001317185.1:c.388+499T>G
(CDH1)
|
NP_001304114.1:n.388+499T>G
|
|
NM_001317186.1:c.-30+499T>G
(CDH1)
|
NP_001304115.1:n.-30+499T>G
|
|
NM_004360.4:c.1936+499T>G
(CDH1)
|
NP_004351.1:n.1936+499T>G
|
|
NM_004360.5:c.1936+499T>G
(CDH1)
MANE Select
|
NP_004351.1:n.1936+499T>G
|
|
NM_001317184.2:c.1753+499T>G
(CDH1)
|
NP_001304113.1:n.1753+499T>G
|
|
NM_001317185.2:c.388+499T>G
(CDH1)
|
NP_001304114.1:n.388+499T>G
|
|
NM_001317186.2:c.-30+499T>G
(CDH1)
|
NP_001304115.1:n.-30+499T>G
|
|