ENST00000329198.5:c.335-162G>A
MANE Select
|
ENSP00000327758.4:n.335-162G>A
|
|
ENST00000329198.4:c.335-162G>A
|
ENSP00000327758.4:n.335-162G>A
|
|
ENST00000424406.2:c.*126G>A
|
ENSP00000395378.2:n.*126G>A
|
|
ENST00000521848.1:c.428G>A
|
ENSP00000427906.1:p.Arg143Gln
|
|
NM_001166175.1:c.*126G>A
|
NP_001159647.1:n.*126G>A
|
|
NM_001166176.1:c.428G>A
|
NP_001159648.1:p.Arg143Gln
|
|
NM_004387.3:c.335-162G>A
|
NP_004378.1:n.335-162G>A
|
|
NM_004387.4:c.335-162G>A
MANE Select
|
NP_004378.1:n.335-162G>A
|
|
NM_001166175.2:c.*126G>A
|
NP_001159647.1:n.*126G>A
|
|
NM_001166176.2:c.428G>A
|
NP_001159648.1:p.Arg143Gln
|
|