ENST00000450056.7:c.1492+56G>A
MANE Select
|
ENSP00000398735.2:n.1492+56G>A
|
|
ENST00000266880.11:c.1405+56G>A
|
ENSP00000266880.8:n.1405+56G>A
|
|
ENST00000315585.11:c.928+56G>A
|
ENSP00000320557.8:n.928+56G>A
|
|
ENST00000432561.6:c.1528+56G>A
|
ENSP00000392395.2:n.1528+56G>A
|
|
ENST00000443047.6:c.1252+56G>A
|
ENSP00000416431.2:n.1252+56G>A
|
|
ENST00000450056.6:c.1492+56G>A
|
ENSP00000398735.2:n.1492+56G>A
|
|
ENST00000535527.5:c.99-2838G>A
|
ENSP00000478791.1:n.99-2838G>A
|
|
ENST00000538235.2:n.59+1869G>A
|
|
|
ENST00000544093.5:c.41+56G>A
|
|
|
ENST00000544268.5:n.791+56G>A
|
|
|
NM_001161344.1:c.1528+56G>A
|
NP_001154816.1:n.1528+56G>A
|
|
NM_001161345.1:c.1525+56G>A
|
NP_001154817.1:n.1525+56G>A
|
|
NM_001161346.1:c.1492+56G>A
|
NP_001154818.1:n.1492+56G>A
|
|
NM_001161347.1:c.1252+56G>A
|
NP_001154819.1:n.1252+56G>A
|
|
NM_018223.2:c.1405+56G>A
|
NP_060693.2:n.1405+56G>A
|
|
NM_001161346.2:c.1492+56G>A
MANE Select
|
NP_001154818.1:n.1492+56G>A
|
|