ENST00000497571.6:c.103-1G>C
MANE Select
|
ENSP00000419923.1:n.103-1G>C
|
|
ENST00000380946.3:n.338-1G>C
|
|
|
ENST00000469435.1:c.103-1G>C
|
ENSP00000419079.1:n.103-1G>C
|
|
ENST00000497571.5:c.103-1G>C
|
ENSP00000419923.1:n.103-1G>C
|
|
ENST00000542957.1:c.103-1G>C
|
ENSP00000445301.1:n.103-1G>C
|
|
NM_001160124.1:c.103-1G>C
|
NP_001153596.1:n.103-1G>C
|
|
NM_001160125.1:c.103-1G>C
|
NP_001153597.1:n.103-1G>C
|
|
NM_001300.5:c.103-1G>C
|
NP_001291.3:n.103-1G>C
|
|
NR_027653.1:n.370-1G>C
|
|
|
NM_001300.6:c.103-1G>C
MANE Select
|
NP_001291.3:n.103-1G>C
|
|
NM_001160124.2:c.103-1G>C
|
NP_001153596.1:n.103-1G>C
|
|
NR_027653.2:n.298-1G>C
|
|
|
NM_001160125.2:c.103-1G>C
|
NP_001153597.1:n.103-1G>C
|
|