ENST00000261769.10:c.163+242T>C
MANE Select
|
ENSP00000261769.4:n.163+242T>C
|
|
ENST00000261769.9:c.163+242T>C
|
ENSP00000261769.4:n.163+242T>C
|
|
ENST00000422392.6:c.163+242T>C
|
ENSP00000414946.2:n.163+242T>C
|
|
ENST00000566510.5:c.163+242T>C
|
ENSP00000458139.1:n.163+242T>C
|
|
ENST00000566612.5:c.163+242T>C
|
ENSP00000454782.1:n.163+242T>C
|
|
ENST00000611625.4:c.163+242T>C
|
ENSP00000481063.1:n.163+242T>C
|
|
ENST00000612417.4:c.163+242T>C
|
ENSP00000478360.1:n.163+242T>C
|
|
ENST00000621016.4:c.163+242T>C
|
ENSP00000480664.1:n.163+242T>C
|
|
NM_004360.3:c.163+242T>C , LRG_301t1:c.163+242T>C
|
NP_004351.1:n.163+242T>C
|
|
NM_001317184.1:c.163+242T>C
|
NP_001304113.1:n.163+242T>C
|
|
NM_001317185.1:c.-1453+242T>C
|
NP_001304114.1:n.-1453+242T>C
|
|
NM_001317186.1:c.-1657+242T>C
|
NP_001304115.1:n.-1657+242T>C
|
|
NM_004360.4:c.163+242T>C
|
NP_004351.1:n.163+242T>C
|
|
NM_004360.5:c.163+242T>C
MANE Select
|
NP_004351.1:n.163+242T>C
|
|
NM_001317184.2:c.163+242T>C
|
NP_001304113.1:n.163+242T>C
|
|
NM_001317185.2:c.-1453+242T>C
|
NP_001304114.1:n.-1453+242T>C
|
|
NM_001317186.2:c.-1657+242T>C
|
NP_001304115.1:n.-1657+242T>C
|
|