ENST00000497571.6:c.676+41G>A
MANE Select
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ENSP00000419923.1:n.676+41G>A
|
|
ENST00000173785.4:n.257+195G>A
|
|
|
ENST00000469435.1:c.717G>A
|
ENSP00000419079.1:p.Gly239=
|
|
ENST00000497571.5:c.676+41G>A
|
ENSP00000419923.1:n.676+41G>A
|
|
ENST00000542957.1:c.676+41G>A
|
ENSP00000445301.1:n.676+41G>A
|
|
NM_001160124.1:c.550+167G>A
|
NP_001153596.1:n.550+167G>A
|
|
NM_001160125.1:c.676+41G>A
|
NP_001153597.1:n.676+41G>A
|
|
NM_001300.5:c.676+41G>A
|
NP_001291.3:n.676+41G>A
|
|
NR_027653.1:n.789+195G>A
|
|
|
NM_001300.6:c.676+41G>A
MANE Select
|
NP_001291.3:n.676+41G>A
|
|
NM_001160124.2:c.550+167G>A
|
NP_001153596.1:n.550+167G>A
|
|
NR_027653.2:n.717+195G>A
|
|
|
NM_001160125.2:c.676+41G>A
|
NP_001153597.1:n.676+41G>A
|
|